Cook Recalls
266 recalls on record · December 1, 1969 to December 29, 2021 · Medical Devices, Vehicles
Recalls by year
69
71
13
14
15
16
17
18
19
20
21
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:
March 21, 2018Medical DevicesFDA
Cook Inc. recalls Central Venous Catheter Tray
Hazard: Label does not state that the product is heparin-coated.
March 21, 2018Medical DevicesFDA
Cook Inc. recalls TFE Coated Curved Newton LLT
Hazard: Label does not state that the product is heparin-coated.
March 21, 2018Medical DevicesFDA
Cook Inc. recalls Rosen Curved Wire Guide
Hazard: Label does not state that the product is heparin-coated.
March 21, 2018Medical DevicesFDA
Cook Inc. recalls Reuter Tip Deflecting Wire Guide
Hazard: Label does not state that the product is heparin-coated.
March 21, 2018Medical DevicesFDA
Cook Inc. recalls Newton Wire Guide
Hazard: Label does not state that the product is heparin-coated.
March 21, 2018Medical DevicesFDA
Cook Inc. recalls Movable Core Wire Guide
Hazard: Label does not state that the product is heparin-coated.
March 21, 2018Medical DevicesFDA
Cook Inc. recalls Fixed Core Wire Guide
Hazard: Label does not state that the product is heparin-coated.
March 21, 2018Medical DevicesFDA
Cook Inc. recalls Fixed Core Bentson
Hazard: Label does not state that the product is heparin-coated.
March 21, 2018Medical DevicesFDA
Cook Inc. recalls Double Flexible Tipped Wire Guide
Hazard: Label does not state that the product is heparin-coated.
March 21, 2018Medical DevicesFDA
Cook Inc. recalls Disposable Reuter Tip Deflecting Wire Guide
Hazard: Label does not state that the product is heparin-coated.
March 21, 2018Medical DevicesFDA
Cook Inc. recalls Coons Interventional Wire Guide
Hazard: Label does not state that the product is heparin-coated.
March 21, 2018Medical DevicesFDA
Cook Inc. recalls Bentson Wire Guide
Hazard: Label does not state that the product is heparin-coated.
March 21, 2018Medical DevicesFDA
Cook Inc. recalls Bentson Plus Wire Guide
Hazard: Label does not state that the product is heparin-coated.
March 21, 2018Medical DevicesFDA
Cook Inc. recalls Bentson Cerebral Wire Guide
Hazard: Label does not state that the product is heparin-coated.
March 21, 2018Medical DevicesFDA
Cook Inc. recalls Amplatz Ultra Stiff Wire Guide
Hazard: Label does not state that the product is heparin-coated.
March 21, 2018Medical DevicesFDA
Cook Inc. recalls Amplatz Stiff Wire Guide
Hazard: Label does not state that the product is heparin-coated.
March 21, 2018Medical DevicesFDA
Cook Inc. recalls Amplatz Extra Stiff Wire Guide
Hazard: Label does not state that the product is heparin-coated.
March 21, 2018Medical DevicesFDA
Cook Inc. recalls Amplatz Extra Stiff Whisker Wire Guide
Hazard: Label does not state that the product is heparin-coated.
March 7, 2018Medical DevicesFDA
Cook Inc. recalls Wills-Oglesby Percutaneous Gastrostomy Set Product Usage: Intended for the percutaneous placement of a catheter for ga
Hazard: Cook has identified that the affected lots may contain wire guides that were loaded backwards into the wire guide holder.
March 7, 2018Medical DevicesFDA
Cook Inc. recalls Percutaneous Gastrojejunostomy Set Product Usage: Intended for the percutaneous placement of a catheter for gastro
Hazard: Cook has identified that the affected lots may contain wire guides that were loaded backwards into the wire guide holder.
March 7, 2018Medical DevicesFDA
Cook Inc. recalls Mallinckrodt Institute Percutaneous Gastrostomy Set Product Usage: Intended for the percutaneous placement of a ca
Hazard: Cook has identified that the affected lots may contain wire guides that were loaded backwards into the wire guide holder.
February 21, 2018Medical DevicesFDA
Cook Inc. recalls Spectrum Central Venous Catheter Tray Minocycline/Rifampin Antibiotic Impregnated, Catalog Identifiers: C-UTLMY-501J-ABR
Hazard: Central venous catheters may not fit over guide wire potentially causing procedure delay.
February 21, 2018Medical DevicesFDA
Cook Inc. recalls Central Venous Tray Triple Lumen Polyurethane Catheter, Catalog Identifier: C-UTLMY-501J-CCT Product Usage: The cent
Hazard: Central venous catheters may not fit over guide wire potentially causing procedure delay.
February 21, 2018Medical DevicesFDA
Cook Inc. recalls Central Venous Catheter Set Heparin Coated Triple Lumen Polyurethane, Catalog Identifiers: C-UTLM-501J-25-6.5-WCE-BH, C-
Hazard: Central venous catheters may not fit over guide wire potentially causing procedure delay.
February 21, 2018Medical DevicesFDA
Cook Inc. recalls Central Venous Catheter Tray Triple Lumen Polyurethane, Catalog Identifier: C-UTLMYJ-501J Product Usage: The central
Hazard: Central venous catheters may not fit over guide wire potentially causing procedure delay.
February 21, 2018Medical DevicesFDA
Cook Inc. recalls Central Venous Catheter Set Triple Lumen Polyurethane, Catalog Identifier: C-UTLM-501J Product Usage: The central ve
Hazard: Central venous catheters may not fit over guide wire potentially causing procedure delay.
June 21, 2017Medical DevicesFDA
Cook Inc. recalls OptiLite Multi-Use Holmium Laser Fibers, Supplied sterilized by ethylene oxide gas in peel-open packages Product Usag
Hazard: Cook Inc. is initiating a voluntary recall of the OptiLite Multi-Use Holmium Laser Fibers because it has been identified that the reprocessing instructions do not provide sufficiently detailed information for the cleaning, disinfection, and sterilization of these products.
June 21, 2017Medical DevicesFDA
Cook Inc. recalls Vue Optic Visualization Source, Flexor Vue Deflecting Endoscopic System, Endoscope, Fiber Optic, Supplied sterilized by
Hazard: Cook Inc. is initiating a voluntary recall of the Vue Optic Visualization Source and the Flexor Vue Deflecting Endoscopic System because it was determined that the current reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products.
June 21, 2017Medical DevicesFDA
Cook Inc. recalls Cook Multi-Use Holmium Laser Fibers, Supplied sterilized by ethylene oxide gas in peel-open packages
Hazard: Correction to the product Instructions for Use because the current reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products.
June 21, 2017Medical DevicesFDA
Cook Inc. recalls Endoscopic Introducer/Extractor
Hazard: reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products