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. 2,807 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,807 in last 12 months

Showing 381400 of 30,087 recalls

Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia Elition S. Product Code (REF): (1) 781357 Recalled by Philips North...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia Ambition X. Product Code (REF): (1) 781356 Recalled by Philips North...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: SmartPath to dStream for XR and 3.0T. Product Code (REF): Recalled by...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Evolution Upgrade 3.0T. Product Code (REF): 782143. MR systems with Recalled...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia Elition X. Product Code (REF): (1) 781358 Recalled by Philips North...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia 3.0T CX. Product Code (REF): 781271. MR systems with Recalled by...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: MR 7700. Product Code (REF): (1) 782120 Recalled by Philips North America...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia 3.0T. Product Code (REF): (1) 781342 Recalled by Philips North...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Evolution Upgrade 1.5T. Product Codes (REF): (1) 782148 Recalled by Philips...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: SmartPath to dStream for 3.0T. Product Code (REF): 782145. MR Recalled by...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia Ambition S. Product Code (REF): 782108. MR systems with Recalled by...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Microbiologics Inc

Recalled Item: KWIK-STIK 2-Pack Recalled by Microbiologics Inc Due to Affected units may...

The Issue: Affected units may fail to recover the target microorganism Campylobacter...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing