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. 2,779 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,779 in last 12 months

Showing 57615780 of 30,087 recalls

Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCurity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCurity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· RoyalVibe Health Ltd.

Recalled Item: CellQuicken Analyzer (Smart-Watch and Software) Recalled by RoyalVibe Health...

The Issue: Ultrasound devices were not authorized, cleared, or approved by FDA, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· AB Sciex, LLC

Recalled Item: Citrine Triple Quad Mass Spectrometer Recalled by AB Sciex, LLC Due to In...

The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· AB Sciex, LLC

Recalled Item: 4500MD Triple Quad Mass Spectrometer Recalled by AB Sciex, LLC Due to In...

The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· AB Sciex, LLC

Recalled Item: API3200MD Mass Spectrometer Recalled by AB Sciex, LLC Due to In rare...

The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· AB Sciex, LLC

Recalled Item: Citrine QTRAP Mass Spectrometer Recalled by AB Sciex, LLC Due to In rare...

The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2023· CooperSurgical, Inc.

Recalled Item: Box as labeled: Regard Recalled by CooperSurgical, Inc. Due to Incorrect...

The Issue: Incorrect component descriptions within the "Contents" section on the Tyvek...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2023· Flower Orthopedics Corporation

Recalled Item: Coventus Flower Orthopedics Flex-Thread TM 3.2mm Cannulated Reamer-used to...

The Issue: Device is breaking while in use, potential for patients to require a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2023· Becton Dickinson Infusion Therapy Systems Inc.

Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems Inc. Due to There is...

The Issue: There is the potential that the safety shield may not properly engage on IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2023· TECHNO-PATH MANUFACTURING LTD.

Recalled Item: Multichem P Recalled by TECHNO-PATH MANUFACTURING LTD. Due to Technopath...

The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2023· TECHNO-PATH MANUFACTURING LTD.

Recalled Item: Multichem S Plus Recalled by TECHNO-PATH MANUFACTURING LTD. Due to...

The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2023· TECHNO-PATH MANUFACTURING LTD.

Recalled Item: Multichem IA Plus Recalled by TECHNO-PATH MANUFACTURING LTD. Due to...

The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...

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

Class II — Potential Health HazardOngoing