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. 2,580 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,580 in last 12 months

Showing 3006130080 of 55,415 recalls

Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
FoodSeptember 18, 2017· Death Wish Coffee Company, LLC

Recalled Item: Death Wish Nitro Canned Cold Brew Coffee 11 oz Recalled by Death Wish Coffee...

The Issue: Potential for Clostridium Botulinum

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 18, 2017· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ Barricor" Lithium Heparin Plasma Blood Collection Tubes for...

The Issue: Increased amount of residual blood present on the top of stopper well after...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2017· MicroPort Orthopedics Inc.

Recalled Item: MicroPort Orthopedics SCHANZ SCREW SELF DRILL Recalled by MicroPort...

The Issue: The item is being recalled due to an inadequate pouch seal. This defect has...

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

Class II — Potential Health HazardOngoing
DrugSeptember 15, 2017· Gadget Island, Inc

Recalled Item: grande X 5800 capsule Recalled by Gadget Island, Inc Due to Undeclared Active

The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 15, 2017· Gadget Island, Inc

Recalled Item: FIFTY SHADES 6000 capsule Recalled by Gadget Island, Inc Due to Undeclared...

The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 15, 2017· Gadget Island, Inc

Recalled Item: PapaZen 3300 capsule Recalled by Gadget Island, Inc Due to Undeclared Active

The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...

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

Class I — Serious Health HazardOngoing
Refund