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MEDICAL ACTION INDUSTRIES INC.

Last updated May 23, 2026

What MEDICAL ACTION INDUSTRIES INC. makes

Medical Action Industries Inc. manufactures single-use surgical and vascular support products, including non-medicated vascular catheterization and maintenance kits, general surgical procedure kits, and peripheral intravenous catheterization support kits. Their portfolio also includes suture kits, suture removal kits, haemodialysis start/stop sets, and vascular access device flush/disinfection tools. The company produces reusable sharp surgical instrument counting trays and pads.

The company’s products are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Medical Action Industries Inc. 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 Medical Action Industries Inc. manufacture?

Medical Action Industries Inc. specializes in single-use surgical and vascular support products. Their portfolio includes non-medicated vascular catheterization and maintenance kits, general surgical procedure kits, peripheral intravenous catheterization support kits, suture kits, suture removal kits, haemodialysis start/stop sets, and vascular access device flush/disinfection tools. They also produce reusable sharp surgical instrument counting trays and pads, which are designed to improve procedural efficiency and safety in clinical settings.

Where is Medical Action Industries Inc. based?

Medical Action Industries Inc. is headquartered in the United States. The company’s location in the US allows it to comply with regional regulatory requirements and serve domestic and potentially international markets where its products are authorized.

Which regulatory registries list Medical Action Industries Inc.’s devices?

Medical Action Industries Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for authorized products, helping healthcare providers and regulators identify and verify the devices in use.

How are Medical Action Industries Inc.’s devices classified under FDA regulations?

Medical Action Industries Inc.’s devices fall under FDA’s Class I and Class II categories. Class I devices generally pose minimal risk and are subject to general controls, while Class II devices require additional performance standards or special controls due to moderate risk. The classification depends on the specific device type and its intended use, as outlined in FDA guidelines.

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

Information

Country: US
Address: —
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 092364462

Catalogue (4362)

Page 1 of 88

Device	Model / Reference	Registries	Class	Status
Medical Action Industries	79580B	FDA UDI	Class II	Active
Medical Action Industries	78734	FDA UDI	Class II	Unknown
Medical Action Industries	78302	FDA UDI	Class II	Unknown
Medical Action Industries	72690C	FDA UDI	Class II	Active
Medical Action Industries	83785	FDA UDI	Class II	Active
Medical Action Industries	73839	FDA UDI	Class I	Active
Medical Action Industries	81144	FDA UDI	Class II	Unknown
Medical Action Industries	57158E	FDA UDI	Class II	Unknown
Medical Action Industries	80400	FDA UDI	Class II	Unknown
Clear Sequence	83592	FDA UDI	Class II	Active
Medical Action Industries	CK1000LH	FDA UDI	Class I	Active
Medical Action Industries	69611B	FDA UDI	Class II	Unknown
Novaplus®	56726	FDA UDI	Class II	Unknown
Medical Action Industries	76659	FDA UDI	Class I	Active
Medical Action Industries	58829	FDA UDI	Class II	Unknown
Medical Action Industries	81183C	FDA UDI	Class II	Unknown
Medical Action Industries	78165B	FDA UDI	Class II	Active
Medical Action Industries	74028	FDA UDI	Class II	Unknown
Medical Action Industries	72574	FDA UDI	Class II	Unknown
Medical Action Industries	73278	FDA UDI	Class II	Unknown
Medical Action Industries	57002	FDA UDI	Class II	Unknown
Medical Action Industries	83541	FDA UDI	Class II	Active
Medical Action Industries	75497B	FDA UDI	Class I	Unknown
Medical Action Industries	NS9210	FDA UDI	Class I	Active
Medical Action Industries	58512	FDA UDI	Class I	Active
Medical Action Industries	75426	FDA UDI	Class II	Unknown
Medical Action Industries	76394	FDA UDI	Class II	Unknown
Medical Action Industries	58599B	FDA UDI	Class II	Active
Medical Action Industries	80643	FDA UDI	Class II	Unknown
Medical Action Industries	57377	FDA UDI	Class II	Unknown
Medical Action Industries	59055	FDA UDI	Class II	Unknown
Medical Action Industries	SM840	FDA UDI	Class II	Unknown
Medical Action Industries	76879	FDA UDI	Class I	Active
Medical Action Industries	80280	FDA UDI	Class II	Unknown
Medical Action Industries	75151	FDA UDI	Class I	Active
Medical Action Industries	56921	FDA UDI	Class II	Unknown
Novaplus®	56679	FDA UDI	Class II	Unknown
Medical Action Industries	EMHP84G	FDA UDI	Class II	Active
Medical Action Industries	83834	FDA UDI	Class II	Active
Medical Action Industries	79506	FDA UDI	Class I	Active
Medical Action Industries	84310	FDA UDI	Class II	Active
Medical Action Industries	59694B	FDA UDI	Class II	Active
Medical Action Industries	80517B	FDA UDI	Class II	Active
Medical Action Industries	61203	FDA UDI	Class II	Active
Medical Action Industries	2106	FDA UDI	Class I	Active
Medical Action Industries	80629E	FDA UDI	Class II	Unknown
Medical Action Industries	77844	FDA UDI	Class II	Active
Medical Action Industries	77317	FDA UDI	Class I	Unknown
Medical Action Industries	79119	FDA UDI	Class II	Unknown
Medical Action Industries	83420	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (37)

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

Medical Action Industries Inc. has 37 recall records initiated between November 6, 2009, and March 17, 2026, with statuses recorded as open, classified, or terminated. The reasons cited include potential sterility compromises—such as breaches of sterile barriers, incomplete seals, or debris—alongside misbranding issues (e.g., incorrect labeling of kits or missing exterior labeling for active ingredients), pH deviations in saline solutions, and mechanical defects (e.g., loose syringe adapters or mismatched expiry dates on components).

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

Date	Recall No.	Class	Status	Reason
Mar 17, 2026	Z-2007-2026	—	open, classified	Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold"
Jun 11, 2024	Z-3129-2024	—	open, classified	The protective pouches were identified to have been improperly labeled with UDI that is associated with an incorrect GMDN (Global Medical Device Nomenclature) code. These blue foam pouches were misused due to misclassification of the GMDN.
Jan 15, 2024	Z-1394-2024	—	open, classified	The kits contain saline flush syringes which were recalled by the supplier.
Nov 4, 2022	Z-0751-2023	—	terminated	XXX
Oct 12, 2022	Z-0765-2023	—	terminated	Scissors contained debris.
Oct 12, 2022	Z-0464-2023	—	terminated	The Port Access Kits were incorrectly labeled as IV Start Kits on the kit label. The case label was correctly labeled as Port Access Kits.
Sep 15, 2022	Z-0265-2023	—	terminated	The kits were incorrectly labeled with an extended expiration date of 02/21/2024 instead of 02/10/2024.
Sep 8, 2021	Z-0147-2022	—	terminated	The ChloraPrep 3ml kit component has a shorter expiry date than the labeled kit expiry date.
May 11, 2021	Z-1946-2021	—	terminated	There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
May 11, 2021	Z-1949-2021	—	terminated	There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
May 11, 2021	Z-1947-2021	—	terminated	There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
May 11, 2021	Z-1945-2021	—	terminated	There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
May 11, 2021	Z-1948-2021	—	terminated	There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
Apr 9, 2021	Z-1557-2021	—	terminated	Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.
Apr 9, 2021	Z-1555-2021	—	terminated	Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.
Apr 9, 2021	Z-1559-2021	—	terminated	Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.
Apr 9, 2021	Z-1554-2021	—	terminated	Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.
Apr 9, 2021	Z-1556-2021	—	terminated	Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.
Apr 9, 2021	Z-1558-2021	—	terminated	Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.
Dec 2, 2019	Z-0779-2020	—	terminated	The kits contain a bottle of saline solution which may exceed the USP specified pH requirements of 4.5-7.0.
Mar 1, 2019	Z-1068-2019	—	terminated	Potential lack of sterility assurance
Nov 27, 2018	Z-0681-2019	—	terminated	Potential compromise of product sterility due to breach of sterile barrier.
Dec 11, 2017	Z-2043-2018	—	terminated	Product sterility potentially compromised.
Apr 19, 2017	Z-2102-2017	—	open, classified	Lint present on sterile Operating Room Towels.
Apr 19, 2017	Z-2101-2017	—	open, classified	Lint present on sterile Operating Room Towels.
Feb 3, 2016	Z-1036-2016	—	terminated	Misbranding; Due to the presence of CHG in the Tegaderm PICC/CVC dressing change convenience kit, which is not identified on the exterior labeling
Jun 12, 2014	Z-1953-2014	—	terminated	Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
Jun 12, 2014	Z-1955-2014	—	terminated	Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
Jun 12, 2014	Z-1957-2014	—	terminated	Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
Jun 12, 2014	Z-1954-2014	—	terminated	Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
Jun 12, 2014	Z-1950-2014	—	terminated	Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
Jun 12, 2014	Z-1952-2014	—	terminated	Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
Jun 12, 2014	Z-1956-2014	—	terminated	Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
Jun 12, 2014	Z-1951-2014	—	terminated	Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
Nov 6, 2009	Z-1074-2010	—	terminated	Manufacturing defect may allow air entry into a central venous catheter, possibly resulting in an air embolism.
Nov 6, 2009	Z-1073-2010	—	terminated	Manufacturing defect may allow air entry into a central venous catheter, possibly resulting in an air embolism.
Nov 6, 2009	Z-1075-2010	—	terminated	Manufacturing defect may allow air entry into a central venous catheter, possibly resulting in an air embolism.