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. 1,908 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
1,908 in last 12 months

Showing 2758127600 of 30,087 recalls

Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Fixed Bearing Partial Knee Cemented Lateral Tibia Size Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Fixed Bearing Partial Knee Cemented Lateral Tibia Size Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Codman & Shurtleff, Inc.

Recalled Item: MedStream Programmable Infusion Pump Recalled by Codman & Shurtleff, Inc....

The Issue: Miscalibrated Fill Level Sensor may affect dosing level

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 7, 2013· Codman & Shurtleff, Inc.

Recalled Item: MedStream Programmable Infusion Pump- Implantable for the intrathecal...

The Issue: Miscalibrated Fill Level Sensor may affect dosing level

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BD BBL BCYE Selective Agar with PAV Recalled by Becton Dickinson & Co. Due...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BD BBL CDC Anaerobe 5% Sheep Blood Agar with Kanamycin and Vancomycin (KV)...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Carestream Health, Inc.

Recalled Item: Carestream DRX-Revolution Mobile X-ray System. Produces radiographic images....

The Issue: Carestream Health Inc. is recalling the power plug on their DRX-Revolution...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Ortho-Clinical Diagnostics

Recalled Item: Colorimetric (CM)/ Rate (RT) incubator wear pads. Product Codes: 1) 6801375...

The Issue: Ortho Clinical Diagnostics is recalling CM/RT wear pads which are a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BD BBL BBE // CDC Anaerobe Laked Sheep Blood Agar with KV Recalled by Becton...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Sybron Dental Specialties

Recalled Item: AOA Mini RPE Screw Assembly Recalled by Sybron Dental Specialties Due to The...

The Issue: The firm initiated the recall of AOA Mini RPE Screw Assembly, because it may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BBL Campylobacter CSM Agar (Charcoal-Based Selective Medium) Recalled by...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BD BBL Schaedler K-V Agar with 5% Sheep Blood Recalled by Becton Dickinson &...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing