Product Recalls in Colorado
Product recalls affecting Colorado — including food, drugs, consumer products, medical devices, and vehicles distributed to Colorado. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,724 recalls have been distributed to Colorado in the last 12 months.
Showing 501–520 of 28,964 recalls
Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Resection Sheath. Model No. A22014A and A22014T. for endoscopic...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Inner Sheath. Model No. A2642. for endoscopic diagnosis and Recalled...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Inner Sheath Recalled by Olympus Corporation of the Americas Due to...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard ORGAN RECOVERY OR PACK Recalled by AVID Medical, Inc. Due to Devices...
The Issue: Devices are not suitable for organ transplant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard ORGAN RECOVERY OR PACK Recalled by AVID Medical, Inc. Due to Devices...
The Issue: Devices are not suitable for organ transplant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard MINI PLUS KIT SOUTH Recalled by AVID Medical, Inc. Due to Devices...
The Issue: Devices are not suitable for organ transplant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEXLOCK Achilles Repair Implant Kits Recalled by Medline Industries, LP Due...
The Issue: There have been multiple complaints of drill bit fusing to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COULTER DxH Diluent Recalled by Beckman Coulter, Inc. Due to Due to specific...
The Issue: Due to specific lots of diluents contributing to elevated platelet Daily...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Da Vinci Product Name: da Vinci X Recalled by Intuitive...
The Issue: Due to a software implementation error that allowed instruments arms failing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Rocket Product Name: Rocket 16Fg Seldinger Catheter Procedure...
The Issue: IFU and device kit labeling contains misleading statements leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Rocket Product Name: Rocket 18Fg Seldinger Catheter Procedure...
The Issue: IFU and device kit labeling contains misleading statements leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Rocket Product Name: Rocket 20Fg Seldinger Catheter Procedure...
The Issue: IFU and device kit labeling contains misleading statements leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter with...
The Issue: IFU and device kit labeling contains misleading statements leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter Procedure...
The Issue: IFU and device kit labeling contains misleading statements leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Rocket Product Name: Rocket 18Fg Seldinger Catheter with...
The Issue: IFU and device kit labeling contains misleading statements leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access 2 Reaction Vessels Recalled by Beckman Coulter, Inc. Due to It has...
The Issue: It has been determined that certain lots of Access 2 Reaction Vessels may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The Recalled...
The Issue: Due to a number of modules flashed with a date and time associated with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm Recalled by C.R. Bard...
The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard InLay Optima Size: 6 Fr. x 14 cm Recalled by C.R. Bard Inc Due to...
The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.