Product Recalls in Ohio
Product recalls affecting Ohio — including food, drugs, consumer products, medical devices, and vehicles distributed to Ohio. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,114 recalls have been distributed to Ohio in the last 12 months.
Showing 13921–13940 of 30,087 recalls
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: 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: 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 6.5x36 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: 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: 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: 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 6.5x105 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 HBS Sterile Lot 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 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 6.5x115 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 TF PET/CT Model # 882456 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: 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: VOLUMAT MC AGILIA US Recalled by Fenwal Inc Due to The firm is correcting...
The Issue: The firm is correcting four software anomalies and KVO (keep vein open) end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vigilant Agilia Recalled by Fenwal Inc Due to The firm is correcting four...
The Issue: The firm is correcting four software anomalies and KVO (keep vein open) end...
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: RX Imola Recalled by Randox Laboratories, Limited Due to There was a report...
The Issue: There was a report of a malfunction with the sensor which resulted in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Daytona Recalled by Randox Laboratories, Limited Due to There was a...
The Issue: There was a report of a malfunction with the sensor which resulted in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core128 Model # 728323 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: iCT Recalled by Philips Medical Systems (Cleveland) Inc Due to In certain...
The Issue: In certain instances when performing a cardiac step and shoot acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.