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. 1,051 recalls have been distributed to Ohio in the last 12 months.
Showing 26241–26260 of 55,415 recalls
Recalled Item: APTIO 9000 STORAGE MODULE Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTIO INPUT/OUTPUT MODULE Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLAB - STORAGE MODULE 9000 Recalled by Siemens Healthcare Diagnostics,...
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TECOTHERM NEO Recalled by Tec Com Gmbh Due to The action is being initiated...
The Issue: The action is being initiated due to potential installation of faulty...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTIO RACK OUTPUT MODULE Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Megestrol Acetate Oral Suspension Recalled by Mckesson Corporation Due to...
The Issue: Supterpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets Recalled by AVKARE Inc. Due to CGMP Deviations: Carcinogen...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets Recalled by AVKARE Inc. Due to CGMP Deviations: Carcinogen...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets Recalled by AVKARE Inc. Due to CGMP Deviations: Carcinogen...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem HCl Extended-release Capsules Recalled by Mylan Institutional,...
The Issue: Failed Impurities/Degradation Specifications; out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets Recalled by AVKARE Inc. Due to CGMP Deviations: Carcinogen...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chocolate Gooey Brownie Ice Cream Recalled by SALT & STRAW LLC Due to...
The Issue: Chocolate Gooey Brownie Ice Cream is recalled due to possible undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: IsoFlex LAL Support Surface Recalled by Stryker Medical Division of Stryker...
The Issue: Certain 2860 IsoFlex LAL support surfaces were assembled with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK(R) 2 AST-P655 Recalled by bioMerieux, Inc. Due to Routine internal...
The Issue: Routine internal review of Device History Records identified six VITEK(R) 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK(R) 2 AST-P640 Recalled by bioMerieux, Inc. Due to Routine internal...
The Issue: Routine internal review of Device History Records identified six VITEK(R) 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVS Aria Cage Recalled by Stryker Spine Due to The anterior and posterior...
The Issue: The anterior and posterior markers on the cage were on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VaccZyme Human Anti-Haemophilus influenza type b Enzyme Immunoassay Kit For...
The Issue: A deterioration of performance was identified with influenza type B Enzyme...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pointe Scientific AutoHDL/LDL Cholesterol Calibrator Recalled by Medtest...
The Issue: Vials of the autoHDL/LDL Calibrator were shipped without a vial label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Smooth Interior Tubing Material: Polyethylene EVA copolymer. This...
The Issue: Some of the Disposable Smooth Interior Tubing may pull apart when stretched.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADAA Cataract Drops Recalled by Westlab Pharmacy, Inc. dba Westlab Pharmacy...
The Issue: Lack of Process Controls
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.