Product Recalls in Idaho
Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,003 recalls have been distributed to Idaho in the last 12 months.
Showing 21481–21500 of 48,215 recalls
Recalled Item: K-Wire HBS Sterile Recalled by BioPro, Inc. Due to Manufacturing flaw in the...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go-EZ Screw 6.5x32 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go-EZ Screw 6.5x36 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire Single Trocar 1.6x150mm Recalled by BioPro, Inc. Due to Manufacturing...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire Single Trocar 2.5x170mm Recalled by BioPro, Inc. Due to Manufacturing...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire Single Trocar 1.1x150mm Recalled by BioPro, Inc. Due to Manufacturing...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go-EZ Screw 6.5x110 Recalled by BioPro, Inc. Due to Manufacturing flaw in...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go-EZ Screw 6.5x100 Recalled by BioPro, Inc. Due to Manufacturing flaw in...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go-EZ Screw 6.5x30 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go-EZ Screw 6.5x38 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go-EZ Screw 6.5x95 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go-EZ Screw 6.5x34 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire Single Trocar 2.5x150mm Recalled by BioPro, Inc. Due to Manufacturing...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go-EZ Screw 6.5x120 Recalled by BioPro, Inc. Due to Manufacturing flaw in...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire Sterile Single Trochar Recalled by BioPro, Inc. Due to Manufacturing...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go-EZ Screw 6.5x115 Recalled by BioPro, Inc. Due to Manufacturing flaw in...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT Recalled by Philips Medical Systems (Cleveland) Inc Due to In...
The Issue: In certain instances when performing a cardiac step and shoot acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IQon Spectral CT Model # 728332 Recalled by Philips Medical Systems...
The Issue: In certain instances when performing a cardiac step and shoot acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 Model # 728231 Recalled by Philips Medical Systems (Cleveland)...
The Issue: In certain instances when performing a cardiac step and shoot acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vereos PET/CT Model # 882446 Recalled by Philips Medical Systems (Cleveland)...
The Issue: In certain instances when performing a cardiac step and shoot acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.