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. 1,904 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
1,904 in last 12 months

Showing 2896128980 of 30,087 recalls

Medical DeviceSeptember 5, 2012· Zimmer, Inc.

Recalled Item: ATS 3000 Automatic Tourniquet System w/HOSES AND LOP SENSOR Intended...

The Issue: Zimmer is conducting a voluntary removal of some Zimmer A.T.S. 3000...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2012· Wright Medical Technology Inc

Recalled Item: Extremity Components: PROTHESE A EXPANSION COMPLETE D=6 LG 12 MM Recalled by...

The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2012· Wright Medical Technology Inc

Recalled Item: Hip Components: INSERT MOBILE "COLLEGIA" TAILLE 58*28 Recalled by Wright...

The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2012· Mindray DS USA, Inc. d.b.a. Mindray North America

Recalled Item: Mindray DPM5 Monitor Recalled by Mindray DS USA, Inc. d.b.a. Mindray North...

The Issue: Mindray has identified an issue with the DPM5 monitors where ST and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard Ventralight ST Mesh. - Ellipse 8" x 10" (20.3 Recalled by Davol, Inc.,...

The Issue: Mislabeled: The 8" x 10" package contains 7" x 9" VENTRALIGHT ST Mesh...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: CLS Stem Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: DTO" Implant Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Dynesys¿ Top-Loading System Cannulated Pedicle + Set Screw Recalled by...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Anatomical Shoulder" Fracture Humeral stem Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Alloclassic SL Shaft Recalled by Zimmer, Inc. Due to Zimmer Inc., is...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: NCB¿ screw ¿ 4.0 self-tapping Recalled by Zimmer, Inc. Due to Zimmer Inc.,...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Anatomical Shoulder" Inverse/Reverse Humeral PE-Insert Sterile Recalled by...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Biolox¿ Option Ceramic Femoral Head System Rx Recalled by Zimmer, Inc. Due...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: zimmer Anatomical Shoulder Glenoid S Recalled by Zimmer, Inc. Due to Zimmer...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Anatomical Shoulder" Inverse Humeral Cup Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Anatomical Shoulder" Inverse/Reverse Glenoid Sterile Recalled by Zimmer,...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Dynesys¿ Revision + set screw Recalled by Zimmer, Inc. Due to Zimmer Inc.,...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: MS-30¿ Stem Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Anatomical Shoulder" Humeral stem Recalled by Zimmer, Inc. Due to Zimmer...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: MS-30¿ Distal centralizer Recalled by Zimmer, Inc. Due to Zimmer Inc., is...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing