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. 2,786 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,786 in last 12 months

Showing 49815000 of 30,087 recalls

Medical DeviceJanuary 3, 2024· Thoratec Corp.

Recalled Item: 1. HeartMate Touch Communication System Recalled by Thoratec Corp. Due to...

The Issue: Due to software and controller systems that results in unexpected pump start...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: SmartPath to dStream for XR and 3.0T. Model (REF) Numbers 781270 Recalled by...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Tornier, Inc

Recalled Item: Stryker Tornier Perform Reversed Glenoid Press-Fit Short Post Ti6AI4V...

The Issue: The incorrect device is contained in the labeled package.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Ingenia 3.0T CX. Model (REF) Numbers 781271 Recalled by Philips North...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Intera 1.5T Achieva Nova-Dual. Model (REF) Number 781173. Recalled by...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Achieva 1.5T. Model (REF) Numbers 781196 Recalled by Philips North America...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: Synapse Cardiology PACS V7.3.0 Recalled by FUJIFILM Healthcare Americas...

The Issue: The LV Mass (2D Bullet) equation may be calculated incorrectly, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Achieva 1.5T Conversion. Model (REF) Numbers 781346 Recalled by Philips...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Intera Achieva 1.5T Pulsar. Model (REF) Number 781171. Recalled by Philips...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Achieva 3.0T. Model. (REF) Numbers 781277 Recalled by Philips North America...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· BALT USA, LLC

Recalled Item: The Prestige Coil System is a product family of embolic Recalled by BALT...

The Issue: Discoloration was identified along the delivery pusher which was attributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Ingenia 1.5T CX. Model (REF) Numbers 781262 Recalled by Philips North...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Achieva 1.5T Initial system. Model (REF) Numbers 781178. Recalled by Philips...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Quidel Corporation

Recalled Item: The Sofia 2 Flu + SARS Antigen FIA employs immunofluorescence Recalled by...

The Issue: One lot of the Sofia 2 Flu + SARS Antigen FIA (Lot 709083) was labelled with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Achieva XR. Model (REF) Numbers 781153 Recalled by Philips North America Due...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: Synapse CV 6. with AR. A web-based application as the Recalled by FUJIFILM...

The Issue: The LV Mass (2D Bullet) equation may be calculated incorrectly, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...

The Issue: Disk Bay may not perform as intended. System may stop functioning and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray Systems Recalled by...

The Issue: Framegrabber card may not perform as intended. Monitor may show no...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...

The Issue: Framegrabber card may not perform as intended. Monitor may show no...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray Systems Recalled by...

The Issue: Disk Bay may not perform as intended. System may stop functioning and...

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

Class II — Potential Health HazardOngoing