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
Valleylab™ Ref VLFT10LSGEN
CO2 Sample Line Intubated Ref QMVAI
General Surgery Procedure Pack Ref NEFRLIMST
Colorectal Surgery Procedure Pack Ref BOX07917V1
Thoracic Surgery Procedure Pack Ref LAPZAKOP1
Bariatric Surgery Procedure Pack Ref BOX04202V1
Bariatric Surgery Procedure Pack Ref BOX04713V8
Bariatric Surgery Procedure Pack Ref BOX02074V1
GYN Surgery Procedure Pack Ref KIT001002ACCGY0
Bariatric Surgery Procedure Pack Ref HAJBAR2
Bariatric Surgery Procedure Pack Ref BOX05381V1
GYN Surgery Procedure Pack Ref BOX04272V1
Reinforced TG W Murphy Eye (MTG) Ref 118-60MTG
GYN Surgery Procedure Pack Ref BOX002503
Bariatric Surgery Procedure Pack Ref BOX02648V3
Thoracic Surgery Procedure Pack Ref BOX07336V1
Bariatric Surgery Procedure Pack Ref BOX07918V1
Breathing Circuit, sterile Ref 305/6722
Thoracic Surgery Procedure Pack Ref US1722I
Bariatric Surgery Procedure Pack Ref BOX04195V1
General Surgery Procedure Pack Ref BREASTKIT03
Bariatric Surgery Procedure Pack Ref BOX02431V2
Bariatric Surgery Procedure Pack Ref BOX02865V1
Bariatric Surgery Procedure Pack Ref BOX09554V2
Electrostatic Filter HME (Sterile) Ref 352/5981
Bariatric Surgery Procedure Pack Ref BOX04641V1
Bariatric Surgery Procedure Pack Ref BOX09425V1
Thoracic Surgery Procedure Pack Ref BOX04966V1
Bariatric Surgery Procedure Pack Ref BOX04656V1
Bariatric Surgery Procedure Pack Ref BOX04784V1
General Surgery Procedure Pack Ref KIT001001ACOVN3
Bariatric Surgery Procedure Pack Ref BOX05424V1
General Surgery Procedure Pack Ref BOX02977V1
Cholecystectomy Procedure Pack Ref BOX07280V1
Bariatric Surgery Procedure Pack Ref BOX01983V3
Cholecystectomy Procedure Pack Ref PST05398V2
Upper GI Surgery Procedure Pack Ref BOX05649V2
Bariatric Surgery Procedure Pack Ref BOX03793V1
Bariatric Surgery Procedure Pack Ref BOX04349V2
Breathing Circuit, sterile Ref 300/6099
Bariatric Surgery Procedure Pack Ref BOX07900V2
Hernia Procedure Pack Ref BOX09444V1
Bariatric Surgery Procedure Pack Ref BOX06965V2
Colorectal Surgery Procedure Pack Ref KIT00952V1
Bariatric Surgery Procedure Pack Ref BOX01199V1
Bariatric Surgery Procedure Pack Ref BOX07039V2
Bariatric Surgery Procedure Pack Ref BOX03016V3
Bariatric Surgery Procedure Pack Ref BOX06604V1
Cholecystectomy Procedure Pack Ref KIT4C1
Bariatric Surgery Procedure Pack Ref BOX06860V3
Showing 1,201-1,250 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.
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- 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
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- 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.
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- 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.