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. 2,597 recalls have been distributed to Ohio in the last 12 months.
Showing 22521–22540 of 55,415 recalls
Recalled Item: Vivitrol (naltrexone for extended-release injectable suspension) 380...
The Issue: Labeling: Not Elsewhere Classified. Drug product kit recalled due to 1 inch...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Keto Farms Keto Snack Mix - Tomato Pepperjack Fruit & Recalled by Keto Farms...
The Issue: California Department of Public Health Inspection found that the allergen,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Keto Farms Keto Snack Mix - Raspberry Gouda Fruit & Recalled by Keto Farms...
The Issue: California Department of Public Health Inspection found that the allergen,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nosh Organic Fruit & Protein Soft Oat Bar Recalled by FIRST START HOLDINGS...
The Issue: Fruit & Protein Soft Oat Bars have the potential to be contaminated with mold.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nosh Organic Fruit & Protein Soft Oat Bar Recalled by FIRST START HOLDINGS...
The Issue: Fruit & Protein Soft Oat Bars have the potential to be contaminated with mold.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Keto Farms Keto Snack Mix - Strawberry Gouda Recalled by Keto Farms LLC Due...
The Issue: California Department of Public Health Inspection found that the allergen,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AQURE basic sytem Recalled by Radiometer Medical ApS Due to The firm has...
The Issue: The firm has become aware that there is a potential problem relating to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FoundationOne CDx test report Recalled by Foundation Medicine, Inc. Due to...
The Issue: Identified potential false positive MSI-H on the test reports provided to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clotrimazole and Betamethasone Dipropionate Cream USP Recalled by Glenmark...
The Issue: Temperature Abuse: Complaints received of liquidy texture.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Superset with 22MM ID Recalled by Intersurgical Inc Due to The port may...
The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Swivel Elbow with Bronchoscopy Port 15MM OD Recalled by Intersurgical...
The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Swivel Elbow with Bronchoscopy Port 15MM OD Recalled by Intersurgical...
The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superset with 22MM ID Recalled by Intersurgical Inc Due to The port may...
The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM - Product Usage: Instrument intended...
The Issue: possibility of the sterility batch being insufficiently sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIMAN DISP.INSTR.ARTICULAT.D:12/440MM Product Usage: Instrument intended...
The Issue: possibility of the sterility batch being insufficiently sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Jarit GEMINI CLAMP 9 1/4 inch - used in Recalled by Integra...
The Issue: A small crack at the box lock corner may after multiple cleaning and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS) for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS) for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Short Fill: fill...
The Issue: Short Fill: fill volume was out of specification at 94 mL (specification: no...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amy's Bowls - Broccoli & Cheddar Bake Recalled by Amys Kitchen Inc Due to...
The Issue: Consumer complaints of black plastic found in product.
Recommended Action: Do not consume. Return to store for a refund or discard.