Covidien llc
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000028763 FEI 1219930
- Devices
- 8,225
- Registrations
- EUDAMEDFDA
- FDA recalls
- 37344 ongoing
Catalogue
Colorectal Surgery Procedure Pack Ref KIT00625V2
Colorectal Surgery Procedure Pack Ref BOX04597V1
Colorectal Surgery Procedure Pack Ref BOX06654V1
Reinforced TG W Murphy Eye (MTG) Ref 118-95MTG
Colorectal Surgery Procedure Pack Ref BOX00814V2
Colorectal Surgery Procedure Pack Ref PST05323V8
Mapelson Breathing Unit, sterile Ref 309/6409
Bariatric Surgery Procedure Pack Ref BOX05491V1
Bariatric Surgery Procedure Pack Ref BOX05783V3
Bariatric Surgery Procedure Pack Ref BOX01374V2
Colorectal Surgery Procedure Pack Ref LAPZD10V
Hernia Procedure Pack Ref BOX00196V1
Cholecystectomy Procedure Pack Ref BOX01515V1
Bariatric Surgery Procedure Pack Ref SPSK139XIII
Bariatric Surgery Procedure Pack Ref BOX05054V1
Bariatric Surgery Procedure Pack Ref BOX08115V1
Bariatric Surgery Procedure Pack Ref BOX08629V1
Bariatric Surgery Procedure Pack Ref KIT00561V
Bariatric Surgery Procedure Pack Ref BOX00609V1
Bariatric Surgery Procedure Pack Ref BOX04861V1
Bariatric Surgery Procedure Pack Ref PST07488
Bariatric Surgery Procedure Pack Ref BOX01875V1
Bariatric Surgery Procedure Pack Ref SPSK148I
Colorectal Surgery Procedure Pack Ref LAPPOLLF19
Bariatric Surgery Procedure Pack Ref WIMLGB2N
Bariatric Surgery Procedure Pack Ref KITSLEEVESIGV2
Nasal cannula Ref 251/5029
Bariatric Surgery Procedure Pack Ref BOX08979V1
Bariatric Surgery Procedure Pack Ref PST01689
Colorectal Surgery Procedure Pack Ref BOX06706V1
Colorectal Surgery Procedure Pack Ref HEMICOLDRLAP
Colorectal Surgery Procedure Pack Ref PST05324V11
Reservoir bags with breathing tube Ref 285/7515
Bariatric Surgery Procedure Pack Ref KITSADISMNROB
Bariatric Surgery Procedure Pack Ref BOX07629V1
Colorectal Surgery Procedure Pack Ref BOX01462V2
Cholecystectomy Procedure Pack Ref KIT00302
Valleylab™ Ref VLFT10LSGEN
Bariatric Surgery Procedure Pack Ref BOX06863V4
Bariatric Surgery Procedure Pack Ref BOX04511V1
GYN Surgery Procedure Pack Ref KIT00168R-1
General Surgery Procedure Pack Ref BOX09525V1
Hernia Procedure Pack Ref BOX07861V4
Hernia Procedure Pack Ref HERUOLDXAR
Thoracic Surgery Procedure Pack Ref BOX07105V2
Appendectomy Procedure Pack Ref BOX09285V2
Bariatric Surgery Procedure Pack Ref BOX08429V1
Bariatric Surgery Procedure Pack Ref PST04077
Bariatric Surgery Procedure Pack Ref BOX08330V1
Colorectal Surgery Procedure Pack Ref BOX08020V1
Showing 1,151-1,200 of 8,225
Company details
- EUDAMED SRN
- US-MF-000028763
- SRN (system / procedure pack)
- US-PR-000013794
- FDA FEI number
- 1219930
- EUDAMED status
- Active
- EUDAMED registered name
- Covidien llc
- Registered address
- 15, Hampshire Street, MA 02048, Mansfield, United States
- Website
- cardinalhealth.com
- [email protected]
- Phone
- +353 57 96 272 69
- PRRC contact
- Linda Zhu
1 more person
- Deep Pal
EUDAMED certificates
3 certificates3 valid, 0 expiredMDR 3next expiry 26 Jun 2027
Notified body 2797 2 certificates
- MDR 728352 Reissued
Quality management system EU MDR
- Issued
- 27 Aug 2026
- Expires
- 31 Aug 2031
- Valid from
- 31 Aug 2026
- MDR 724712 Supplemented
Quality management system EU MDR
- Issued
- 25 Sep 2026
- Expires
- 11 Aug 2031
- Reason
- Other
DNV Product Assurance AS 2460 1 certificate
- 10000481938-PA-NoMA-DNK Amended
Quality management system EU MDR
- Issued
- 16 Jul 2026
- Expires
- 26 Jun 2027
- Reason
- Mnf data change
FDA recalls
Recalls initiated per year
- 2017 22
- 2018 25
- 2019 44
- 2020 24
- 2021 26
- 2022 12
- 2023 9
- 2024 8
- 2025 3
- 2026 7
2026
- 13 May 2026 Z-2950-2026 Class II Ongoing Due to products are incorrectly flagged as expired due to the system's 24-hour usage limit, rendering the product unavailable for clinical procedures.
Full distribution text
- 23 Apr 2026 Z-2271-2026 Class II Ongoing Temperature probe devices lack FDA clearance.
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- 23 Apr 2026 Z-2272-2026 Class II Ongoing Temperature probe devices lack FDA clearance.
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- 23 Apr 2026 Z-2273-2026 Class II Ongoing Temperature probe devices lack FDA clearance.
Full distribution text
- 23 Apr 2026 Z-2653-2026 Class II Ongoing Due to product labeling incorrectly including the symbol indicating non-DEHP (Bis(2-ethylhexyl) phthalate as the product includes 30 to 35% DEHP.
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- 15 Apr 2026 Z-2261-2026 Class II Ongoing Due to customer complaint regarding incorrect display box labeling.
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- 30 Jan 2026 Z-1557-2026 Class II Ongoing Due to complaints and investigations stating that alarms from the primary patient bedside monitor was not alarming/being transmitted and received on the remote patient monitoring system.
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- 13 May 2026 Z-2950-2026 Class II Ongoing Due to products are incorrectly flagged as expired due to the system's 24-hour usage limit, rendering the product unavailable for clinical procedures.
2025
- 23 Jun 2025 Z-2151-2025 Class II Ongoing Bedside SpO2 Patient Monitoring System alarms not heard/recognized, resulting in: treatment delay, lack of low oxygen saturation response, respiratory failure, arrhythmia. Highlighting operator's manual: 1)For patient Safety don't silence/decrease alarm volume, 2)Sensor off alarm (no perfusion detected) is low priority alarm, 3)Set monitors to Homecare Mode outside of hospital/professional setting
Full distribution text
- 21 May 2025 Z-1915-2025 Class I Ongoing Ventilator Printed Circuit Board Assembly may have two separate capacitors that may fail, which may result in the ventilator either shutting down during use, thus necessitating use of an alternate form of ventilation, or the shutdown alert alarm fails to alarm effectively during shut down, which may result in respiratory failure, hypoventilation, low oxygen saturation, hypoxia, treatment delay.
Full distribution text
- 26 Feb 2025 Z-1390-2025 Class I Ongoing Tracheostomy tube with cuff reusable inner cannula has a flange that may disconnect from the outer cannula of the device, which could cause respiratory failure, aspiration, unspecified tissue injury, aspiration, respiratory tract infection, bronchospasm, a delay to treatment and/or death.
Full distribution text
- 23 Jun 2025 Z-2151-2025 Class II Ongoing Bedside SpO2 Patient Monitoring System alarms not heard/recognized, resulting in: treatment delay, lack of low oxygen saturation response, respiratory failure, arrhythmia. Highlighting operator's manual: 1)For patient Safety don't silence/decrease alarm volume, 2)Sensor off alarm (no perfusion detected) is low priority alarm, 3)Set monitors to Homecare Mode outside of hospital/professional setting
Show the 25 most recent of 373 recalls
2024
- 9 Jul 2024 Z-2636-2024 Class I Ongoing Battery management system within Laryngoscope devices may deplete below the deign threshold which may result in thermal event followed by risk of explosion.
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- 9 Jul 2024 Z-2637-2024 Class I Ongoing Battery management system within Laryngoscope devices may deplete below the deign threshold which may result in thermal event followed by risk of explosion.
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- 9 Jul 2024 Z-2717-2024 Class II Ongoing IFU update to address device's battery handling information.
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- 24 Jun 2024 Z-2446-2024 Class I Ongoing Any single affected ventilator should only be used for the 10- year labelled service life, but if longer ventilatory support is required using more than one ventilator over time, the use of these devices for more than 14 years of cumulative duration may pose harm to health due to a volatile organic compound (VOC), 2-propanol, 1,3-dichloro released from some components in the ventilator gas pathway
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- 25 Apr 2024 Z-2038-2024 Class II Ongoing Due to saline conductivity issues, their is a potential that dilation catheters may provide inaccurate esophageal diameter measurements that may lead to various harms.
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- 21 Feb 2024 Z-1330-2024 Class II Ongoing Packs including 5 laparotomy sponges may contain incorrect product with a blue loop, X-ray detectable feature, and ethylene oxide treatment; however, this incorrect product wasn't steam pre-treated prior to sterilization, and has no RF tag, which if non-sterile, may lead to infection, tissue trauma, and sepsis, and if in the scannable area, would lead a "CLEAR" display.
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- 9 Jan 2024 Z-1731-2024 Class II Ongoing manufacturing defects to sensor cable connectors may result in error codes or non-functioning channel
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- 9 Jan 2024 Z-1732-2024 Class II Ongoing manufacturing defects to sensor cable connectors may result in error codes or non-functioning channel
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- 9 Jul 2024 Z-2636-2024 Class I Ongoing Battery management system within Laryngoscope devices may deplete below the deign threshold which may result in thermal event followed by risk of explosion.
2023
- 16 Nov 2023 Z-0631-2024 Class II Ongoing Due to software issue, New systems may exhibit an error which may prohibit use of new systems resulting in system being inoperable
- 28 Sep 2023 Z-0144-2024 Class I Ongoing Defective video laryngoscopes that did not pass quality tests established for the product, that were designated for destruction, were stolen, and subsequently distributed for sale. Defective device use may result in failed laryngoscopy and/or intubation.
- 22 Aug 2023 Z-2651-2023 Class II Ongoing Inadequate internal fixation of the power inlet port to the cuff pressure manager device causes the external power inlet to became dislodged within the device housing after several uses, which prevents the device from being charged, and could lead to treatment delay.
- 10 Aug 2023 Z-0168-2024 Class II Ongoing Laryngoscope blades may contain an ineffective application of anti-fog agent which may result in condensation accumulating causing the screen to be blurred or obscured.
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- 10 Aug 2023 Z-0169-2024 Class II Ongoing Laryngoscope blades may contain an ineffective application of anti-fog agent which may result in condensation accumulating causing the screen to be blurred or obscured.
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- 2 Jun 2023 Z-2282-2023 Class II Ongoing Cell Collection Device may be at increased risk of the sponge detaching from the string during removal of the device from the patient, which could lead to device fragments in patient, obstruction, airway obstruction, secondary intervention, secondary intervention (with the primary procedure), supraglottic airway obstruction, and aspiration.
Full distribution text
- 22 May 2023 Z-2008-2023 Class II Ongoing Single ILLUMISITE Platform Console was converted from a 220-240VAC model to a 120VAC configuration using a non-supplied power cord and non-supplied fuses in the field by Medtronic Field Service Engineer.
FDA establishments
- Covidien TIJUANA, B.C. Mexico · MX FEI 3002807391
- Covidien - Galway(County) · IE FEI 3002807850
- Covidien - Santo Domingo · DO FEI 3003495548
What Covidien llc makes
Covidien LLC manufactures reusable device sterilization and disinfection containers, single-use basic endotracheal tubes, and secretion suction kits. Their portfolio includes sterile surgical procedure packs for gynecological, bariatric, appendectomy, colorectal, and thoracic surgeries, as well as silicone Foley catheters and breathing circuits with reservoir bags. Electrostatic filters are also part of their product line.
The company’s devices are classified under EU regulations as Class I, Class IIa, Class IIb, and Class III, with listings maintained in the EUDAQMED database. Covidien LLC is based in the United States.
Frequently asked questions
How many devices does Covidien llc have in the registry?
The registry currently lists 8225 devices for Covidien llc. Devices recorded under merged duplicate company entries are counted once.
Are there FDA recall records for Covidien llc?
FDA recall records list 373 recalls initiated by Covidien llc, the most recent initiated on 2026-05-13. 74 of them are recorded as ongoing. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What EUDAMED certificates are recorded for Covidien llc?
EUDAMED lists 3 certificates for Covidien llc (quality management system) under MDR. The most recent was issued on 2026-09-25.
Which FDA establishments are linked to Covidien llc?
3 FDA establishments are linked to Covidien llc in the registry; they are listed on the company page.