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Howmedica Osteonics Corp.

United States·US-MF-000001881

Last updated September 18, 2026

What Howmedica Osteonics Corp. makes

The company manufactures reusable orthopaedic instruments for positioning implants during knee and hip surgeries, including tibial and femoral trial components for knee prostheses. It also produces acetabular liners—both non-constrained and constrained polyethylene—and prefabricated acetabular trial components for hip replacements, as well as reusable tibial inserts for knee implants.

These devices are classified under FDA regulations as Class I, Class II, and Class III, with all products listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Howmedica Osteonics Corp. manufacture?

Howmedica Osteonics Corp. specializes in reusable orthopaedic instruments and components used during knee and hip surgeries. Their products include positioning instruments for implant placement, tibial and femoral trial components for knee prostheses, acetabular liners (both non-constrained and constrained polyethylene), prefabricated acetabular trial components for hip replacements, and tibial inserts for knee implants. These devices are designed to assist surgeons in achieving precise implant alignment and fit.

Where is Howmedica Osteonics Corp. based?

Howmedica Osteonics Corp. is headquartered in the United States. The company’s location in the US aligns with regulatory frameworks governing medical device manufacturing, distribution, and compliance in North America.

Which regulatory registries list devices manufactured by Howmedica Osteonics Corp?

Devices produced by Howmedica Osteonics Corp. are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for each device’s identification, classification, and regulatory status under FDA guidelines.

How are the devices manufactured by Howmedica Osteonics Corp. classified under FDA regulations?

The devices produced by Howmedica Osteonics Corp. fall under three FDA device classes: Class I (generally low-risk devices), Class II (devices requiring special controls to ensure safety and effectiveness), and Class III (high-risk devices requiring premarket approval). The classification depends on factors like the device’s intended use, potential risks, and the body area it interacts with, such as orthopaedic implants or surgical instruments.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
United States
Address
325, Corporate Drive , Mahwah, United States
LinkedIn
—
Facebook
—
Phone
201-831-5000
PRRC Contact
Dervillia Murphy
EUDAMED SRN
US-MF-000001881
FDA FEI Number
—
DUNS Number
058311945

Catalogue (16214)

Page 1 of 325
DeviceModel / ReferenceRegistriesClassStatus
Instrument 7555-0008
FDA UDI
Class IActive
Secur-Fit J6052-1240
FDA UDI
Class IIActive
Abg 4845-0106
FDA UDI
Class IIActive
Secur-Fit 2051-2056
FDA UDI
Class IIActive
Instrument I-K39600510
FDA UDI
Class IIActive
Unix 4540-0410
FDA UDI
Class IIActive
Secur-Fit 1601-08127
FDA UDI
Class IIActive
Secur-Fit 2051-2060P
FDA UDI
Class IIActive
Triathlon 5513-F-702
FDA UDI
Class IIActive
Instrument I-K2812BC06
FDA UDI
Class IIActive
Instrument 6481-8-101
FDA UDI
Class IActive
Instrument 7002-0150
FDA UDI
Class IIActive
Instrument 4845-2-918
FDA UDI
Class IActive
Instrument I-K2034060L
FDA UDI
Class IActive
Instrument I-H0689HA28
FDA UDI
Class IActive
System 12 6302-H-222
FDA UDI
Class IIActive
Triathlon 5530-G-213-E
FDA UDI
Class IIActive
Instrument I-K42041430
FDA UDI
Class IActive
Trident Ii 700-04-52E
FDA UDI
Class IIActive
Trident 661-00-28H
FDA UDI
Class IIActive
Instrument 6210-2-100
FDA UDI
Class IActive
Scorpio 72-26-0512
FDA UDI
Class IIActive
Triathlon 5531-G-716-E
FDA UDI
Class IIActive
Instrument I-K2919KF02
FDA UDI
Class IIActive
Specialty Triathlon Ts Trial Assessment Guide Size 1 Right I-K4275TGR1
FDA UDI
Class IIActive
Series 7000 7492-0308
FDA UDI
Class IIActive
Triathlon 5530-G-014-E
FDA UDI
Class IIActive
Triathlon 5530-G-509-E
FDA UDI
Class IIActive
Trident X3 Insert 763-10-32G
FDA UDI
Class IIActive
Instrument I-K3103PR08
FDA UDI
Class IUnknown
Instrument 6264-8-044R
FDA UDI
Class IIActive
Instrument 6278-4-450
FDA UDI
Class IActive
Instrument 7650-3363
FDA UDI
Class IActive
Trident 621-10-32H
FDA UDI
Class IIActive
Centrax 6226-2-242
FDA UDI
Class IIActive
Instrument I-H1385TP0G
FDA UDI
Class IIUnknown
Secur-Fit 2051-2054
FDA UDI
Class IIActive
Accolade 6721-0535
FDA UDI
Class IIActive
Instrument 6304-6-350
FDA UDI
Class IActive
Accolade 6720-0635
FDA UDI
Class IIActive
Instrument I-K0912DC27
FDA UDI
Class IActive
Instrument 2250-32F
FDA UDI
Class IIActive
Instrument 6541-8-130
FDA UDI
Class IActive
Instrument 6481-1-301
FDA UDI
Class IActive
Instrument 4845-5-525
FDA UDI
Class IActive
Tritanium 500-03-60F
FDA UDI
Class IIActive
Omnifit 6088-0935-200L
FDA UDI
Class IIActive
Trident X3 Insert 723-00-36E
FDA UDI
Class IIActive
Instrument 1601-5007
FDA UDI
Class IActive
Instrument 8050-0002
FDA UDI
Class IActive

Related Companies

Authorised Representatives

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (100)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Howmedica Osteonics Corp. has 233 recall records spanning from November 12, 2002, to February 2, 2026, with statuses recorded as open, classified, or terminated. The recalls involve issues such as software error messages preventing device activation, mismatched custom-made devices, potential product mix-ups in labeling, incorrect expiry dates, distortion from repeated autoclaving, oversized internal profiles in certain components, detachment risks in packaging, loosening screws, overhanging device parts, and mechanical failures like locking mechanism malfunctions or fractured components. Reasons include manufacturing defects, labeling errors, and design or material-related concerns.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

DateRecall No.ClassStatusReason
Feb 2, 2026Z-1572-2026—open, classified

A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment. These screws, which secure the cover to the Angled Saw Housing, may loosen during use and detach from the attachment.

Nov 12, 2025Z-0963-2026—open, classified

When the device is activated during surgery, the device software issues an error message "Instrument Face Mask (6001385000000) is not valid for this application" resulting in an inability to use the device.

Aug 28, 2025Z-2640-2025—open, classified

a potential product mix where the package labeled as Catalog Number 0580-1-442, lot A00976, may contain Catalog Number 0580-1-352, lot G8754849, and vice versa. Patient labels may also be impacted.

Sep 4, 2024Z-0023-2025—open, classified

Anterior locking tabs on the Triathlon Universal Baseplate are out of specification which may prevent engagement of either of the two locking tabs with the locking wire of the tibial insert.

Aug 7, 2024Z-0044-2025—open, classified

Stryker has identified an issue with the characterization process that impacted the constant values assigned to the associated MICS Handpieces.

Aug 5, 2024Z-2732-2024—open, classified

A patient specific, custom-made device was supplied for a surgical procedure that did not match the design proposal.

Jun 19, 2024Z-2372-2024—open, classified

Mislabeled: the size on the package label of the UNITRAX Endoprosthesis Head Component potentially may not match the device within the packaging. This product mix only involves the three (3) sizes (43mm, 42mm, and the 38mm)

Jun 19, 2024Z-2370-2024—open, classified

Mislabeled: the size on the package label of the UNITRAX Endoprosthesis Head Component potentially may not match the device within the packaging. This product mix only involves the three (3) sizes (43mm, 42mm, and the 38mm)

Jun 19, 2024Z-2371-2024—open, classified

Mislabeled: the size on the package label of the UNITRAX Endoprosthesis Head Component potentially may not match the device within the packaging. This product mix only involves the three (3) sizes (43mm, 42mm, and the 38mm)

May 23, 2024Z-2153-2024—open, classified

The design of the HRIS Storage & Sterilization Case and Tray P/N 6210-9-900 and the Gray Revision Instrument System Accessory Tray/Case P/N 6210-9-910 may lead to misuse of the Gray Revision Instruments including re-use and re-sterilization of the single-use, sterile-packaged instruments.

May 23, 2024Z-2152-2024—open, classified

The design of the HRIS Storage & Sterilization Case and Tray P/N 6210-9-900 and the Gray Revision Instrument System Accessory Tray/Case P/N 6210-9-910 may lead to misuse of the Gray Revision Instruments including re-use and re-sterilization of the single-use, sterile-packaged instruments.

Feb 27, 2024Z-1624-2024—open, classified

The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell

Feb 27, 2024Z-1628-2024—open, classified

The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell

Feb 27, 2024Z-1621-2024—open, classified

The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell

Feb 27, 2024Z-1627-2024—open, classified

The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell

Feb 27, 2024Z-1623-2024—open, classified

The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell

Feb 27, 2024Z-1622-2024—open, classified

The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell

Feb 27, 2024Z-1629-2024—open, classified

The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell

Feb 27, 2024Z-1631-2024—open, classified

The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell

Feb 27, 2024Z-1632-2024—open, classified

The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell

Feb 27, 2024Z-1626-2024—open, classified

The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell

Feb 27, 2024Z-1625-2024—open, classified

The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell

Feb 27, 2024Z-1630-2024—open, classified

The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell

Feb 6, 2024Z-1261-2024—open, classified

Potential packaging breaches of inner blister and outer sterile blister.

Feb 6, 2024Z-1260-2024—open, classified

Potential packaging breaches of inner blister and outer sterile blister.

Feb 6, 2024Z-1259-2024—open, classified

Potential packaging breaches of inner blister and outer sterile blister.

Feb 6, 2024Z-1263-2024—open, classified

Potential packaging breaches of inner blister and outer sterile blister.

Feb 6, 2024Z-1262-2024—open, classified

Potential packaging breaches of inner blister and outer sterile blister.

Feb 6, 2024Z-1265-2024—open, classified

Potential packaging breaches of inner blister and outer sterile blister.

Feb 6, 2024Z-1264-2024—open, classified

Potential packaging breaches of inner blister and outer sterile blister.

Feb 6, 2024Z-1266-2024—open, classified

Potential packaging breaches of inner blister and outer sterile blister.

Dec 22, 2023Z-1000-2024—open, classified

Failed to meet the acceptance criteria for the seal integrity and/or package integrity testing for the Sterile Barrier Outer Pouch and the Protective Barrier Inner Pouch, compromising product sterility

Dec 22, 2023Z-0999-2024—open, classified

Failed to meet the acceptance criteria for the seal integrity and/or package integrity testing for the Sterile Barrier Outer Pouch and the Protective Barrier Inner Pouch, compromising product sterility

Dec 1, 2023Z-0918-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0883-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0878-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0906-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0896-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0917-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0884-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0919-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0879-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0904-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0892-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0887-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0869-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0910-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0893-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0905-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0922-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0886-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0907-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0900-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0873-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0874-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0871-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0902-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0881-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0901-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0875-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0913-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0877-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0916-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0921-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0903-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0898-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0889-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0894-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0912-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0897-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0915-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0891-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0890-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0885-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0924-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0899-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0908-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0909-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0895-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0911-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0888-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0926-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0876-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0914-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0923-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0882-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0870-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0880-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0872-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0925-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Dec 1, 2023Z-0920-2024—open, classified

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

May 3, 2023Z-1921-2023—open, classified

The Exeter V40 Trial Head, catalog number 6364-8-026 (size 26mm, -3) may appear green, when it is meant to be a blue color. Green signifies a size 26mm, +3 Trial Head.

Apr 13, 2023Z-1653-2023—open, classified

Mislabeled:Labeled Catalog Number: 5531-G-312-E, TRIATHLON X3 TIBIAL BEARING INSERT CS #3 12MM, may contain Catalog Number: 5532-G-413-E, TRIATHLON X3 TIBIAL BEARING INSERT PS #4 13MM, and vice versa

Apr 13, 2023Z-1654-2023—open, classified

Mislabeled:Labeled Catalog Number: 5531-G-312-E, TRIATHLON X3 TIBIAL BEARING INSERT CS #3 12MM, may contain Catalog Number: 5532-G-413-E, TRIATHLON X3 TIBIAL BEARING INSERT PS #4 13MM, and vice versa

Mar 10, 2023Z-1386-2023—open, classified

Certain lots of the Restoris MultiCompartmental Knee (MCK) Tibial Baseplate Trials contain product with incorrect size laser marking

Mar 10, 2023Z-1385-2023—open, classified

Ccertain lots of the Restoris MultiCompartmental Knee (MCK) Tibial Baseplate Trials contain product with incorrect size laser marking

Nov 7, 2022Z-0737-2023—open, classified

Instructions for Use (IFU) included in the packaging is missing a translation in the Turkish language. Although the Turkish translation is missing, all content within the IFUs is accurate.

Nov 7, 2022Z-0736-2023—open, classified

Instructions for Use (IFU) included in the packaging is missing a translation in the Turkish language. Although the Turkish translation is missing, all content within the IFUs is accurate.

Oct 21, 2022Z-0240-2023—open, classified

Simplex HV With Gentamicin CE, 10 PACKS (P/N 6193-1-010) were distributed to customers who had ordered Simplex HV With Gentamicin in US, 10 PACKS (P/N 6195-1-010)

Aug 24, 2022Z-1778-2022—open, classified

A MK4 Tibial Bearing was supplied with the intention to mate with the Tibial Metal Casing in-situ. However, the device in-situ was a MK3 Tibial Metal Casing. The supplied MK4 tibial bearing was not exchangeable for the MK3 tibial bearing. The surgeon needed to complete the surgery by re-assembling and re-inserting the extracted MK3 tibial bearing.