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.

55,415 total recalls
2,609 in last 12 months

Showing 2126121280 of 55,415 recalls

FoodNovember 26, 2019· Fuji Food Products, Inc.

Recalled Item: Okami brand 8pc Salmon Philly Roll Recalled by Fuji Food Products, Inc. Due...

The Issue: RTE products potentially contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 26, 2019· Fuji Food Products, Inc.

Recalled Item: Okami brand 25pcs Sushi Platter Recalled by Fuji Food Products, Inc. Due to...

The Issue: RTE products potentially contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 25, 2019· Apothecus Pharmaceutical Corp.

Recalled Item: VCF Vaginal Contraceptive Foam Recalled by Apothecus Pharmaceutical Corp....

The Issue: Defective Delivery System: canister unit exhibiting propellant leakage or...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 25, 2019· Medisca, Inc.

Recalled Item: Estriol Recalled by Medisca, Inc. Due to Failed Impurities/Degradation...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 25, 2019· AuroMedics Pharma LLC

Recalled Item: Vancomycin Hydrochloride for Injection Recalled by AuroMedics Pharma LLC Due...

The Issue: Discoloration: Product complaints of discoloration after reconstitution of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 25, 2019· OraLabs, Incorporated

Recalled Item: Petroleum jelly (White Petrolatum) USP 100% Recalled by OraLabs,...

The Issue: Cross contamination with other products: undeclared contaminants of phenol...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 25, 2019· GE Healthcare, LLC

Recalled Item: Carestation 620/650/650c A2 Product Usage: anesthesia systems are intended...

The Issue: GE Healthcare has become aware that there is a potential for a loose cable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 25, 2019· GE Healthcare, LLC

Recalled Item: Carestation 620/650/650c A1 Product Usage: anesthesia systems are intended...

The Issue: GE Healthcare has become aware that there is a potential for a loose cable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 25, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Cios Alpha Recalled by Siemens Medical Solutions USA, Inc Due to During a...

The Issue: During a routine inspection of a system, a crack on the C-arm holder was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2019· Greiner Bio-One North America, Inc.

Recalled Item: VACUETTE TUBE Recalled by Greiner Bio-One North America, Inc. Due to The...

The Issue: The Vacuette 3.5mL Serup Sep Clot Activator Tubes may have been damaged at...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2019· Vyaire Medical

Recalled Item: bellavista 1000 ventilator Recalled by Vyaire Medical Due to The G6...

The Issue: The G6 bellavista 1000 US ventilators may experience intermittent failures:...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2019· Zest Anchors LLC

Recalled Item: LOCATOR OVERDENTURE IMPLANT SYSTEM STERILE R Rx Only QTY 1 . Recalled by...

The Issue: The abutment provided with the Implant System may be out of specification,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodNovember 22, 2019· Whole Foods Market

Recalled Item: Whole Foods Market Raspberry Cheesecake Italian Gelato 1 Pint (473mL)...

The Issue: Undeclared egg

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 22, 2019· Elekta Inc

Recalled Item: Monaco Radiation Treatment Planning System (RTP) System Recalled by Elekta...

The Issue: Monaco is using the incorrect energy when optimizing and calculating dose.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2019· Caire, Inc.

Recalled Item: CAIRE MODEL: FreeStyle Comfort Oxygen Concentrator - Product Usage: The...

The Issue: Four units of European version FreeStyle Comfort were distributed in the US,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2019· DeRoyal Industries Inc

Recalled Item: DeRoyal KNEE BRACE Recalled by DeRoyal Industries Inc Due to The Warrior...

The Issue: The Warrior Recovery Knee Brace has the potential to come apart due to the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2019· Stryker GmbH

Recalled Item: Stryker Pin To Rod Coupling External Fixation System Hoffmann II Recalled by...

The Issue: Pin To Rod Coupling could not clamp the pin and rod as intended

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2019· STANLEY BLACK & DECKER INC.

Recalled Item: The products involved are DeWALT laser distance measurers Recalled by...

The Issue: The products are labeled as Class II lasers. However, the level of laser...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2019· 3M Company - Health Care Business

Recalled Item: 3M Durapore Advanced Recalled by 3M Company - Health Care Business Due to...

The Issue: While the product meets all safety and efficacy criteria, long term exposure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2019· Medtronic Inc.

Recalled Item: Medtronic MiniMed 620G 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.

Class I — Serious Health HazardOngoing