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. 2,624 recalls have been distributed to Ohio in the last 12 months.
Showing 19141–19160 of 55,415 recalls
Recalled Item: Lisinopril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: Presence of Foreign Tablets/Capsules: Lisinopril Tablets USP, 20mg found in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Giant Eagle Dried Island Fruit Mix Recalled by Giant Eagle Due to Undeclared...
The Issue: Giant Eagle, Inc. has issued a voluntary recall of Giant Eagle Dried Island...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Restore Clinician Programmer Application Software Recalled by Medtronic...
The Issue: The original version of the A71100 Restore Clinician Programmer Application...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Match Point System The Match Point System is intended to Recalled by...
The Issue: The procedure side indicated in the top header of the Shoulder Case Planning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cytocell LPH533-A NUP98 Distal Probe Green - Product Usage:The NUP98...
The Issue: A low risk of a false positive result being issued with a laboratory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Anti-SARS-CoV-2 IgG Reagent Pack Recalled by Ortho Clinical...
The Issue: The reagent bottles may be swapped within the reagent pack, which may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Anti-SARS-CoV-2 Total Reagent Recalled by Ortho Clinical Diagnostics...
The Issue: The reagent bottles may be swapped within the reagent pack, which may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dietary supplements Recalled by Provident Nutraceutical div. of Ortho...
The Issue: Various branded dietary supplements may contain undeclared soy.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Model No:T-SPOT.TB8 Recalled by Oxford Immunotec Due to Incorrect expiration...
The Issue: Incorrect expiration date included in test kit labeling and/or in Substrate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No:T-SPOT.TB50 Recalled by Oxford Immunotec Due to Incorrect...
The Issue: Incorrect expiration date included in test kit labeling and/or in Substrate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: uEXPLORER PET/CT Diagnostic Imaging System - Product Usage: This system...
The Issue: 1) 1) Potential intermittent issue may cause image data problems, may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: uMI 550 PET/CT Diagnostic Imaging System - Product Usage: This Recalled by...
The Issue: 1) Service function problem may cause false marking of a bad channel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial knee prosthesis Recalled by Smith & Nephew, Inc. Due to Due to an...
The Issue: Due to an inconsistency in the raw material process, specific lots may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pointts sistema de ellmlnact! Recalled by OraSure Technologies, Inc. Due to...
The Issue: Unit boxes not properly sealed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Personelle OTC Skin Tag Remover Recalled by OraSure Technologies, Inc. Due...
The Issue: Unit boxes not properly sealed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVS Advanced Wart Remover Kit Recalled by OraSure Technologies, Inc. Due to...
The Issue: Unit boxes not properly sealed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SINGLES Carbide US-No. FG556 Recalled by Hager & Meisinger Gmbh Due to...
The Issue: US-dates between the product package label and the bar code display.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAstat-Dx Respiratory SARS-CoV-2 Panel (US IVD under FDA Recalled by Qiagen...
The Issue: There is an increased rate of potential false positive results for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Models FR4A-SPR-BO US -...
The Issue: The product contains a non-functional component not in product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Model FR4A-TRL-AO US -...
The Issue: The product contains a non-functional component not in product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.