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. 2,609 recalls have been distributed to Ohio in the last 12 months.
Showing 21281–21300 of 55,415 recalls
Recalled Item: Medtronic MiniMed 670G System with SmartGuard Recalled by Medtronic Inc. Due...
The Issue: There have been reported incidents of a loose reservoir that can no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX Recalled by Radiometer Medical ApS Due to The analyzers fail on...
The Issue: The analyzers fail on S7950 (Range +) QC measurements due to the hemolyzer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 640G Insulin Infusion Pump Recalled by Medtronic Inc. Due...
The Issue: There have been reported incidents of a loose reservoir that can no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX PLUS Recalled by Radiometer Medical ApS Due to The analyzers fail...
The Issue: The analyzers fail on S7950 (Range +) QC measurements due to the hemolyzer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 630G System with SmartGuard Recalled by Medtronic Inc. Due...
The Issue: There have been reported incidents of a loose reservoir that can no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frog Hollow Holiday Fruitcake Incorrect ingredients: Organic butter Recalled...
The Issue: Customer alerted firm that walnuts were listed on the web page but not in...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: EXPAREL Recalled by Pacira Pharmaceuticals, Inc. Due to Sub Potent Drug: Out...
The Issue: Sub Potent Drug: Out of Specification (OOS)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mirtazapine Tablets Recalled by AuroMedics Pharma LLC Due to Labeling: Label...
The Issue: Labeling: Label Error on Declared Strength; cases labelled Mirtazapine 15mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mirtazapine Tablets Recalled by AuroMedics Pharma LLC Due to Labeling: Label...
The Issue: Labeling: Label Error on Declared Strength; cases labelled Mirtazapine 15mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SURE 48hr Confidence Unscented Original Solid Anti-Perspirant & Deodorant...
The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant...
The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ranitidine Tablets Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Potential N-Nitrosodimethylamine (NDMA) amounts above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SURE 48hr Confidence Regular Original Solid Anti-Perspirant & Deodorant Net...
The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SURE 48hr Confidence Nourishing Coconut invisible solid Antiperspirant &...
The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Outlook Safety Infusion System Y-type Blood Set Recalled by B. Braun...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Introducer Sets Maquet 8 Fr. Recalled by Datascope Corporation...
The Issue: Potential for compromised sterility in breached pouches of specific lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Introducer Sets Maquet 7 Fr. Recalled by Datascope Corporation...
The Issue: Potential for compromised sterility in breached pouches of specific lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safeline Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safeline Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.