Covidien Recalls
493 recalls on record · June 27, 2012 to August 19, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
Also filed under
The recall feeds record what looks like the same company under more than one name:
February 11, 2015Medical DevicesFDA
Covidien recalls Covidien Trellis-6 Peripheral Infusion System. Models BVT608010V01, BVT608030V01, BVT612010V01, and BVT612030V01. Ster
Hazard: A manufacturing error resulted in the risk of incorrect proximal and distal balloon inflation port identification on the units. Units have been identified to have the distal balloon inflation port incorrectly labeled as proximal, and, the proximal balloon port incorrectly labeled as distal.
October 22, 2014Medical DevicesFDA
Covidien LLC recalls Philips HEARTSTART Multifunction Electrode Pads Part Number: M3718A
Hazard: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs
October 22, 2014Medical DevicesFDA
Covidien LLC recalls MediChoice¿ Multifunction Electrode Part Number: MC171 OH
Hazard: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs
October 22, 2014Medical DevicesFDA
Covidien LLC recalls Covidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number: 40000006
Hazard: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs
October 22, 2014Medical DevicesFDA
Covidien LLC recalls Covidien Kendall Adult Multi-Function Defibrillation Electrodes Part Number: 20660
Hazard: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs
October 22, 2014Medical DevicesFDA
Covidien LLC recalls Coviden Medi-Trace Cadence Adult Multi-Function Defibrillation Electrodes, Pre-connected Part Number: 22660PC
Hazard: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs
October 22, 2014Medical DevicesFDA
Covidien LLC recalls Covidien Medi-Trace Cadence and Kendall Adult Multi-Function Defibrillation Electrodes, Radiotransparent Part Number: 2
Hazard: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs Defibrillators
July 16, 2014Medical DevicesFDA
Covidien LLC recalls Devon Supine, Lithotomy and Trendelenburg Positioning Kit; Product Code: 31151090 Product Usage: The device is inten
Hazard: Straps may separate from the foam pad.
January 15, 2014Medical DevicesFDA
Covidien recalls Puritan Bennett 840 ventilator systems software part number 4-070212-85, revision AB-AG. The intended use of the prod
Hazard: Covidien is conducting a voluntary field corrective action on Puritan Bennett 840 ventilator systems with certain software revisions in response to customer reports of ventilator diagnostic code XB0069 in which the device stops mechanical ventilation due to a software error.
September 18, 2013Medical DevicesFDA
Covidien LLC recalls Monoject 100 Units/mL Heparin Lock Flush, 12 mL Syringe with 5 mL Fill Product ID: 8881590125 Product Usage: Both
Hazard: Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin
September 18, 2013Medical DevicesFDA
Covidien LLC recalls Monoject 100 Units/mL Heparin Lock Flush, 12 mL Syringe with 3 mL Fill Product ID: 8881590123 Product Usage: Both 0
Hazard: Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin
September 18, 2013Medical DevicesFDA
Covidien LLC recalls Monoject 100 Units/mL Heparin Lock Flush, 12 mL Syringe with 10 mL Fill Product ID: 8881590121 Product Usage: Both
Hazard: Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin
September 18, 2013Medical DevicesFDA
Covidien LLC recalls Monoject 10 Units/mL Heparin Lock Flush, 12 mL Syringe with 5 mL Fill Product ID: 8881580125 Product Usage: Both 0.
Hazard: Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin
September 18, 2013Medical DevicesFDA
Covidien LLC recalls Monoject 10 Units/mL Heparin Lock Flush, 12 mL Syringe with 3 mL Fill Product ID: 8881580123 Product Usage: Both 0.
Hazard: Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin
September 18, 2013Medical DevicesFDA
Covidien LLC recalls Monoject 10 Units/mL Heparin Lock Flush, 12 mL Syringe with 10 mL Fill Product ID:8881580121 Product Usage: Both 0.
Hazard: Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin
September 18, 2013Medical DevicesFDA
Covidien LLC recalls Monoject 0.9% Sodium Chloride Flush Syringe, 12 mL Syringe with 5 mL Fill Product ID: 8881570125 Product Usage: Bot
Hazard: Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin
September 18, 2013Medical DevicesFDA
Covidien LLC recalls Monoject 0.9% Sodium Chloride Flush Syringe, 12 mL Syringe with 3 mL Fill Product ID: 8881570123 Product Usage: Bot
Hazard: Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin
September 18, 2013Medical DevicesFDA
Covidien LLC recalls Monoject 0.9% Sodium Chloride Flush Syringe, 12 mL Syringe with 10 mL Fill Product ID: 8881570121 Product Usage: Bo
Hazard: Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin
June 12, 2013Medical DevicesFDA
Covidien LP recalls Versaport Bladeless Optical Fixation Cannula - 5mm Product Code: ONBFCA5ST The Versaport" Bladeless Optical 5mm troc
Hazard: Seals may disengage from the cannula which may result in a component inadvertently disengaging into the patients cavity
June 12, 2013Medical DevicesFDA
Covidien LP recalls Versaport Bladeless Optical Fixation Cannula - 5mm Short Product Code: ONBFCA5SH The Versaport" Bladeless Optical
Hazard: Seals may disengage from the cannula which may result in a component inadvertently disengaging into the patients cavity
June 12, 2013Medical DevicesFDA
Covidien LP recalls Versaport Bladeless Optical Trocar With (2) Fixation Cannulae - 5mm Product Code: ONB5STF2C The Versaport" Bladele
Hazard: Seals may disengage from the cannula which may result in a component inadvertently disengaging into the patients cavity
June 12, 2013Medical DevicesFDA
Covidien LP recalls Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Product Code: ONB5STF The Versaport" Bladeless Optica
Hazard: Seals may disengage from the cannula which may result in a component inadvertently disengaging into the patients cavity
June 12, 2013Medical DevicesFDA
Covidien LP recalls Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Short Product Code: ONB5SHF The Versaport" Bladeles
Hazard: Seals may disengage from the cannula which may result in a component inadvertently disengaging into the patients cavity
June 12, 2013Medical DevicesFDA
Covidien LP recalls Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Long Product Code: ONB5LGF The Versaport" Bladeless
Hazard: Seals may disengage from the cannula which may result in a component inadvertently disengaging into the patients cavity
May 22, 2013Medical DevicesFDA
Covidien LLC recalls Curity Staple Remover Kit; Product Code: 66701. Staple Remover Kit.
Hazard: On March 26, 2013 Covidien received a recall notice from one of their suppliers CareFusion. CareFusion is recalling a variety of OTC drug products including the 10% Povidone Iodine SEPP Applicator which is utilized in specific convenience kits.
May 22, 2013Medical DevicesFDA
Covidien LLC recalls Curity I.V. Start Kit, Product ID: 80530 and Curity I.V. Start Kit Product ID: 8508. IV Start Kit.
Hazard: On March 26, 2013 Covidien received a recall notice from one of their suppliers CareFusion. CareFusion is recalling a variety of OTC drug products including the 10% Povidone Iodine SEPP Applicator which is utilized in specific convenience kits.
May 8, 2013Medical DevicesFDA
Covidien LLC recalls Medi-Trace Cadence Pediatric Radiotransparent Defibrillation Electrode Product ID: 22550P. Intended for use in cardi
Hazard: Defibrillation Electrodes may arc/spark result in thermal damage to the leadwire, which could render the device incapable of delivering the appropriate energy or shock to the patient
May 8, 2013Medical DevicesFDA
Covidien LLC recalls Medi-Trace Cadence Adult Radiotransparent Defibrillation Electrode Product ID: 22550R. Intended for use in cardiover
Hazard: Defibrillation Electrodes may arc/spark result in thermal damage to the leadwire, which could render the device incapable of delivering the appropriate energy or shock to the patient
April 17, 2013Medical DevicesFDA
Covidien LP recalls Covidien Endo GIA AutoSuture Universal Loading Unit, 30mm-2.0mm Product Code: 030450 Ap
Hazard: Single Use Loading Unit contained two staples loaded in each cartridge pocket and may result in difficulty firing and removing the device from the application site, which may require medical intervention
October 3, 2012Medical DevicesFDA
Covidien LP recalls Covidien Duet TRS 60 4.8 mm Universal Articulating Single Use Loading Unit. Product Code: DUET6048A. Single Use Load
Hazard: Duet TRS may have the potential to injure adjacent anatomical structures which may result in life threatening post-operative complications.