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. 2,561 recalls have been distributed to Ohio in the last 12 months.
Showing 34141–34160 of 55,415 recalls
Recalled Item: DF Coated Integral Shaft & Stem 15x30x38 Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Shaft L=120mm Recalled by Stanmore Implants Worldwide Ltd. Due to...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Component Metal Cased Small Long Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INOVA (benzoyl peroxide) 4% Recalled by Cipher Pharmaceuticals US LLC Due to...
The Issue: Subpotent Drug: Product label claim is 4% Benzoyl Peroxide, Initial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT Recalled by...
The Issue: A breach in the sterile packaging may have occurred resulting in potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Electrophysiology Catheter Cables Catalog Number: CB3434CT...
The Issue: A breach in the sterile packaging may have occurred resulting in potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyberKnife Robotic Radiosurgery Systems Recalled by Accuray Incorporated Due...
The Issue: Accuray has become aware of a potential safety issue involving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPT Croutons is a synthetic bone substitute designed for the Recalled by...
The Issue: OPT Croutons, part number 65-0210-S, is recalled due to the result of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentasa (mesalamine) Controlled-Release Capsules Recalled by Shire PLC Due...
The Issue: Presence of Foreign Tablets/Capsules; 500 mg capsules were found in bottles...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: A1CNow SELF CHECK (European) Recalled by Polymer Technology Systems Due to A...
The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVS Health At Home A1C Test Kit Recalled by Polymer Technology Systems Due...
The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A1CNow+ Systems (professional use product) Recalled by Polymer Technology...
The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ReliOn FastA1C Test Recalled by Polymer Technology Systems Due to A...
The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Walgreens At-Home A1C Test Kit Recalled by Polymer Technology Systems Due to...
The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Special Connector Instruments (Special Connector Recalled by K2M, Inc...
The Issue: Instruments were developed without adequate consideration given to the need...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Radiology 12.2 - Picture Archive Communication System (PACS)...
The Issue: Issue for customers that use an EMR login or legacy web URL login or legacy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bariatric Bed - BARPKG-IVC 1633 Recalled by Invacare Corporation Due to A...
The Issue: A quality issue with the junction box used in the bariatric bed junction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Junction Box - 1104343 and 1193560 Recalled by Invacare Corporation Due to A...
The Issue: A quality issue with the junction box used in the bariatric bed junction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bariatric Bed - BAR600IVC Recalled by Invacare Corporation Due to The...
The Issue: The junction box used in the bariatric bed may emit sparks and result in a fire.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Section - BAR5490IVC Recalled by Invacare Corporation Due to A quality...
The Issue: A quality issue with the junction box used in the bariatric bed junction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.