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:
June 10, 2020Medical DevicesFDA
Covidien Llc recalls Multifire Endo Hernia 0 12mm Stapler with 4.0mm Disposable Loading Unit , Part No. 174027 - Product Usage: has applicati
Hazard: The product is recalled due to a manufacturing assembly error that may cause the staples to fail to properly advance within the staple cartridge when the instrument handle is compressed.
June 10, 2020Medical DevicesFDA
Covidien Llc recalls Multifire Endo Hernia 0 12mm Stapler with 4.8mm Disposable Loading Unit , Part No. 174025 - Product Usage: has applicati
Hazard: The product is recalled due to a manufacturing assembly error that may cause the staples to fail to properly advance within the staple cartridge when the instrument handle is compressed.
June 10, 2020Medical DevicesFDA
Covidien Llc recalls Multifire VersaTrack Auto Suture Hernia Stapler, 4.8mm, Part No. 174023 - Product Usage: has application in endoscopic g
Hazard: The product is recalled due to a manufacturing assembly error that may cause the staples to fail to properly advance within the staple cartridge when the instrument handle is compressed.
June 10, 2020Medical DevicesFDA
Covidien Llc recalls Multifire VersaTrack Auto Suture Hernia Stapler, 4.0mm, Part No. 174021 - Product Usage: has application in endoscopic g
Hazard: The product is recalled due to a manufacturing assembly error that may cause the staples to fail to properly advance within the staple cartridge when the instrument handle is compressed.
May 20, 2020Medical DevicesFDA
Covidien Llc recalls Dover 400 ml 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley Tray, 18 Fr/Ch (6.0 mm), 5 mL Catheter Pre-c
Hazard: Temperature sensing catheters failed to meet the established calibrated temperature sensing tolerance of +/- 0.2¿C. Failure to correctly measure patient body temperatures could lead to an incorrect diagnosis and insufficient treatment
May 20, 2020Medical DevicesFDA
Covidien Llc recalls Dover 400 ml 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley Tray,18 Fr/Ch (6.0 mm), 5 mL Catheter Pre-co
Hazard: Temperature sensing catheters failed to meet the established calibrated temperature sensing tolerance of +/- 0.2¿C. Failure to correctly measure patient body temperatures could lead to an incorrect diagnosis and insufficient treatment
May 20, 2020Medical DevicesFDA
Covidien Llc recalls Dover 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley Tray 400mL, 16 Fr/Ch (5.3 mm), 5 mL Catheter Pre-c
Hazard: Temperature sensing catheters failed to meet the established calibrated temperature sensing tolerance of +/- 0.2¿C. Failure to correctly measure patient body temperatures could lead to an incorrect diagnosis and insufficient treatment
May 20, 2020Medical DevicesFDA
Covidien Llc recalls Dover 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley Tray 400mL, Premium, Urine Meter, 16 Fr/Ch (5.3 mm)
Hazard: Temperature sensing catheters failed to meet the established calibrated temperature sensing tolerance of +/- 0.2¿C. Failure to correctly measure patient body temperatures could lead to an incorrect diagnosis and insufficient treatment
May 20, 2020Medical DevicesFDA
Covidien Llc recalls Dover 400mL, 100% Silicone Premium Urine Meter Foley Tray, 16 Fr/Ch (5.3 mm), 5 mL Catheter Pre-connected to 2000 mL Dr
Hazard: Temperature sensing catheters failed to meet the established calibrated temperature sensing tolerance of +/- 0.2¿C. Failure to correctly measure patient body temperatures could lead to an incorrect diagnosis and insufficient treatment
May 20, 2020Medical DevicesFDA
Covidien Llc recalls Dover 100% Silicone Premium Urine Meter Tray 400mL, 16 Fr/Ch (5.3 mm), 5 mL Foley Catheter Pre-connected to 2000 mL Drai
Hazard: Temperature sensing catheters failed to meet the established calibrated temperature sensing tolerance of +/- 0.2¿C. Failure to correctly measure patient body temperatures could lead to an incorrect diagnosis and insufficient treatment
May 20, 2020Medical DevicesFDA
Covidien Llc recalls Dover 100% Silicone Premium Urine Meter Foley Tray, 400mL, 14 Fr/Ch (4.7 mm), 5 mL Catheter Pre-connected to 2000 mL Dra
Hazard: Temperature sensing catheters failed to meet the established calibrated temperature sensing tolerance of +/- 0.2¿C. Failure to correctly measure patient body temperatures could lead to an incorrect diagnosis and insufficient treatment
May 20, 2020Medical DevicesFDA
Covidien Llc recalls Dover 100% Silicone Silver-Hydrogel Coated Foley Catheter with Temperature Sensor 18FR 5CCCC2W, Product Code: 50518ICT -
Hazard: Temperature sensing catheters failed to meet the established calibrated temperature sensing tolerance of +/- 0.2¿C. Failure to correctly measure patient body temperatures could lead to an incorrect diagnosis and insufficient treatment
May 20, 2020Medical DevicesFDA
Covidien Llc recalls Dover 100% Silicone Foley Catheter with Temperature 16FR 5CC2W, Product Code: 50516T - Product Usage: for Drainage of t
Hazard: Temperature sensing catheters failed to meet the established calibrated temperature sensing tolerance of +/- 0.2¿C. Failure to correctly measure patient body temperatures could lead to an incorrect diagnosis and insufficient treatment
May 20, 2020Medical DevicesFDA
Covidien Llc recalls Dover 100% Silicone Silver-Hydrogel Coated Foley Catheter with Temperature Sensor 16FR 5CCCC2W, Product Code: 50516ICT
Hazard: Temperature sensing catheters failed to meet the established calibrated temperature sensing tolerance of +/- 0.2¿C. Failure to correctly measure patient body temperatures could lead to an incorrect diagnosis and insufficient treatment
May 20, 2020Medical DevicesFDA
Covidien Llc recalls Dover 100% Silicone Foley Catheter with Temperature Sensor 14FR 5CC2W, Product Code: 50514T - Product Usage: for Draina
Hazard: Temperature sensing catheters failed to meet the established calibrated temperature sensing tolerance of +/- 0.2¿C. Failure to correctly measure patient body temperatures could lead to an incorrect diagnosis and insufficient treatment
March 11, 2020Medical DevicesFDA
Covidien Llc recalls Kits containing Covidien Force TriVerse Electrosurgical Devices. Distributed in EMEA (Europe, Middle East, and Africa) o
Hazard: Sterile packaging may potentially be compromised, and use of products may result in increased risk for infection.
March 11, 2020Medical DevicesFDA
Covidien Llc recalls Covidien Force TriVerse Electrosurgical Devices, Product numbers FT3000 and FT3000DB, UDI 10884524000084 20884524000081
Hazard: Sterile packaging may potentially be compromised, and use of products may result in increased risk for infection.
February 26, 2020Medical DevicesFDA
Covidien LLC recalls Biosyn Monofilament Absorbable Suture 6/0 30" VIOLET CV-23, Item Code UM201
Hazard: There is a potential for packaging integrity issues impacting the humidity or sterility barrier of specific production lots.
February 26, 2020Medical DevicesFDA
Covidien LLC recalls Polysorb Braided Absorbable Suture 2/0 30"VIOLET GU-46, Item Code UL878 - Product Usage: Indicated for use in soft tissu
Hazard: There is a potential for packaging integrity issues impacting the humidity or sterility barrier of specific production lots.
February 26, 2020Medical DevicesFDA
Covidien LLC recalls Polysorb Braided Absorbable Suture 0 30" VIOLET GU-46, Item Code UL877 - Product Usage: Indicated for use in soft tissue
Hazard: There is a potential for packaging integrity issues impacting the humidity or sterility barrier of specific production lots.
February 26, 2020Medical DevicesFDA
Covidien LLC recalls Polysorb Braided Absorbable Suture 4/0 30 VIOLET CVF23, Item Code UL203 - Product Usage: Indicated for use in soft tissu
Hazard: There is a potential for packaging integrity issues impacting the humidity or sterility barrier of specific production lots.
February 26, 2020Medical DevicesFDA
Covidien LLC recalls Polysorb Braided Absorbable Suture 4/0 30 VIO SC-2 124K, Item Code SL654 - Product Usage: Indicated for use in soft tiss
Hazard: There is a potential for packaging integrity issues impacting the humidity or sterility barrier of specific production lots.
February 26, 2020Medical DevicesFDA
Covidien LLC recalls Polysorb Braided Absorbable Suture UD 4/0 18 P-13, Item Code SL5690 - Product Usage: Indicated for use in soft tissue ap
Hazard: There is a potential for packaging integrity issues impacting the humidity or sterility barrier of specific production lots.
February 26, 2020Medical DevicesFDA
Covidien LLC recalls Polysorb Braided Absorbable Suture UD 3/0 30 P-14, Item Code SL5679 - Product Usage: Indicated for use in soft tissue ap
Hazard: There is a potential for packaging integrity issues impacting the humidity or sterility barrier of specific production lots.
February 26, 2020Medical DevicesFDA
Covidien LLC recalls Polysorb Braided Absorbable Suture 6/0 18" UNDYED P-10, Item Code SL1625G - Product Usage: Indicated for use in soft tis
Hazard: There is a potential for packaging integrity issues impacting the humidity or sterility barrier of specific production lots.
February 26, 2020Medical DevicesFDA
Covidien LLC recalls Polysorb Braided Absorbable Suture 6-0 18" UNDYED SS-24 D/A, Item Code L2752K - Product Usage: Indicated for use in soft
Hazard: There is a potential for packaging integrity issues impacting the humidity or sterility barrier of specific production lots.
February 26, 2020Medical DevicesFDA
Covidien LLC recalls Polysorb Braided Absorbable Suture 6/0 12"" VL SS-24 D/A, Item Code L1742K - Product Usage: Indicated for use in soft ti
Hazard: There is a potential for packaging integrity issues impacting the humidity or sterility barrier of specific production lots.
February 26, 2020Medical DevicesFDA
Covidien LLC recalls Polysorb Braided Absorbable Suture 3/0 30" UNDYED V-20, Item Code GLS322 - Product Usage: Indicated for use in soft tiss
Hazard: There is a potential for packaging integrity issues impacting the humidity or sterility barrier of specific production lots.
February 26, 2020Medical DevicesFDA
Covidien LLC recalls Polysorb Braided Absorbable Suture 2-0 UNDYED 30" V-20, Item Code GL323 - Product Usage: Indicated for use in soft tissu
Hazard: There is a potential for packaging integrity issues impacting the humidity or sterility barrier of specific production lots.
February 26, 2020Medical DevicesFDA
Covidien LLC recalls Polysorb Braided Absorbable Suture 2/0 UNDYED 30" V-30 (75CM), Item Code GL228 - Product Usage: Indicated for use in sof
Hazard: There is a potential for packaging integrity issues impacting the humidity or sterility barrier of specific production lots.