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 2552125540 of 55,415 recalls

FoodOctober 23, 2018· ASK Foods Inc

Recalled Item: ASK Foods Inc. Naturally Creative Firecracker Slaw Recalled by ASK Foods Inc...

The Issue: Products recalled due to potential contamination with Listeria monocytogenes...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 23, 2018· ASK Foods Inc

Recalled Item: ASK Foods Inc. Rigatoni Casserole Recalled by ASK Foods Inc Due to Potential...

The Issue: Products recalled due to potential contamination with Listeria monocytogenes...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 23, 2018· ASK Foods Inc

Recalled Item: ASK Foods Inc. Naturally Creative Recalled by ASK Foods Inc Due to Potential...

The Issue: Products recalled due to potential contamination with Listeria monocytogenes...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 23, 2018· ASK Foods Inc

Recalled Item: Taste of Inspirations Rotini Salad Recalled by ASK Foods Inc Due to...

The Issue: Products recalled due to potential contamination with Listeria monocytogenes...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 23, 2018· ASK Foods Inc

Recalled Item: Wegmans Roasted Corn and Bean Salad Recalled by ASK Foods Inc Due to...

The Issue: Products recalled due to potential contamination with Listeria monocytogenes...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2018· Janssen Pharmaceuticals, Inc.

Recalled Item: Ortho-Novum 7/7/7 (norethindrone/ethinyl/estradiol) Tablets Recalled by...

The Issue: Labeling: Incorrect Instructions; Instructions included for use with the...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2018· Janssen Pharmaceuticals, Inc.

Recalled Item: Ortho-Novum 1/35 (norethindrone/ethinyl estradiol) Tablets Recalled by...

The Issue: Labeling: Incorrect Instructions; Instructions included for use with the...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 22, 2018· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Catapres .2 (clonidine hydrochloride Recalled by Boehringer Ingelheim...

The Issue: Failed Dissolution Specifications: OOS resultsduring routine stability testing

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire - Bullet Tip Recalled...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Neusoft Medical Systems Co., Ltd.

Recalled Item: NeuViz 16 Essence Multi-slice CT Scanner System Product Usage: The Recalled...

The Issue: Software defect: For Helical scan with ClearView function, when small arc...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail¿ System - Tear Drop Guide Wire Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail¿ System - Tear Drop Guide Wire Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Becton Dickinson & Co.

Recalled Item: BD BBL Trypticase Soy Agar with 5% Sheep Blood Recalled by Becton Dickinson...

The Issue: a portion of a single lot was not manufactured in accordance with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail¿ System - Tear Drop Guide Wire Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer M/DN¿ Intramedullary Fixation Humeral Guide Wire - Bullet Tip...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Vanguard Knee System -PS Open Box Femoral Right Recalled by Zimmer Biomet,...

The Issue: Label on the outer carton or the patient labels does not match label on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Vanguard Knee System -PS Open Box Femoral Left Recalled by Zimmer Biomet,...

The Issue: Label on the outer carton or the patient labels does not match label on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· bioMerieux, Inc.

Recalled Item: VITEK 2 Antimicrobial Susceptibility Testing (AST) using one or more...

The Issue: False resistant results for Streptococcus anginosus and Streptococcus...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Neusoft Medical Systems Co., Ltd.

Recalled Item: NeuViz 128 Multi-slice CT Scanner System Product Usage: The Multi-Slice...

The Issue: Software defect: For Helical scan with ClearView function, when small arc...

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

Class II — Potential Health HazardOngoing