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. 2,487 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,487 in last 12 months

Showing 4506145080 of 55,415 recalls

Medical DeviceSeptember 30, 2014· CooperSurgical, Inc.

Recalled Item: CooperSurgical MILEX PESSARY KITS-Ring w/Support Folding Pessary- #1 Model:...

The Issue: Incorrect expiration date printed on the MILEX PESSARY KIT packaging

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

Class III — Low RiskOngoing
Medical DeviceSeptember 30, 2014· Masimo Corporation

Recalled Item: Masimo SET uSpO2 Cable The Masimo SET uSpO2 Pulse Oximetry Recalled by...

The Issue: Firm has identified a small number of Oximetry Cables with crossed-internal...

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

Class II — Potential Health HazardOngoing
FoodSeptember 30, 2014· Ikea North America Srvcs Inc

Recalled Item: Elk shaped pasta Ekologiska PASTA-ALGAR FULLKORN Pasta elks wholemeal...

The Issue: Pasta-Algar and Pasta-Algar Fullkorn are recalled due to undeclared soy.

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 30, 2014· Ikea North America Srvcs Inc

Recalled Item: Elk shaped pasta Ekologiska PASTA-ALGAR Pasta elks Recalled by Ikea North...

The Issue: Pasta-Algar and Pasta-Algar Fullkorn are recalled due to undeclared soy.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 29, 2014· Merge Healthcare, Inc.

Recalled Item: Merge Healthcare Recalled by Merge Healthcare, Inc. Due to It has been...

The Issue: It has been reported that during use, the SpO2 value displayed on the Hemo...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2014· Integra LifeSciences Corp.

Recalled Item: Integra Selector Kit Sterile single use device A bi-lumen Recalled by...

The Issue: Some specific lots of Selector Tubing may potentially leak irrigation fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2014· Coloplast Manufacturing US, LLC

Recalled Item: Coloplast Conveen Urine Collection Leg Bag Recalled by Coloplast...

The Issue: Coloplast is recalling the Conveen Contour Leg Bag due to potential leakage...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2014· Smiths Medical ASD, Inc.

Recalled Item: CADD-Solis Medication Safety Software Recalled by Smiths Medical ASD, Inc....

The Issue: Smiths Medical has identified an issue with a single batch (Lot Number...

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

Class II — Potential Health HazardOngoing
DrugSeptember 29, 2014· Baxter Healthcare Corp.

Recalled Item: DOPamine Hydrochloride and 5% Dextrose INJ Recalled by Baxter Healthcare...

The Issue: Lack of Assurance of Sterility: A small cut in the solution bag may have...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2014· Forest Pharmaceuticals Inc

Recalled Item: Bystolic (nebivolol) tablets Recalled by Forest Pharmaceuticals Inc Due to...

The Issue: Failed Dissolution Specification; at the 6-month stability time point

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2014· Actavis Laboratories, FL, Inc.

Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...

The Issue: Failed Tablet/Capsule Specifications: Presence of split or broken tablets.

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2014· Sun Pharma Global Inc.

Recalled Item: Venlafaxine Hydrochloride Extended-Release Tablets Recalled by Sun Pharma...

The Issue: Failed Dissolution Specifications; 12 month stability time point

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 26, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Calibrator E Recalled by Siemens Healthcare Diagnostics, Inc Due to...

The Issue: Positive bias for Calibrator E lot kits ending in 38 and 39 with the ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2014· Biomet, Inc.

Recalled Item: Green Mamba Suture Passer. The Biomet Sports Medicine Mamba instruments...

The Issue: An investigation identified that high level friction may exist between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2014· Amerx Health Care Corp.

Recalled Item: Amerigel Hydrogel Wound Dressing Wound management Recalled by Amerx Health...

The Issue: Formulation deviation

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2014· Biomet, Inc.

Recalled Item: Mamba Disposable Nitinol Needle. The Biomet Sports Medicine Mamba...

The Issue: An investigation identified that high level friction may exist between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2014· Amerx Health Care Corp.

Recalled Item: Amerigel Post-op Surgical Kits Wound management Recalled by Amerx Health...

The Issue: Formulation deviation

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2014· Amerx Health Care Corp.

Recalled Item: Amerigel Daily Dressing Packets Wound management Recalled by Amerx Health...

The Issue: Formulation deviation

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2014· Biomet, Inc.

Recalled Item: Black Mamba Suture Passer. The Biomet Sports Medicine Mamba instruments...

The Issue: An investigation identified that high level friction may exist between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2014· Amerx Health Care Corp.

Recalled Item: Amerigel Saturated Gauze Dressing Wound management Recalled by Amerx Health...

The Issue: Formulation deviation

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

Class II — Potential Health HazardOngoing