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. 1,787 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
1,787 in last 12 months

Showing 4506145080 of 55,415 recalls

Medical DeviceSeptember 30, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension HB1C Flex reagent cartridge Recalled by Siemens Healthcare...

The Issue: Certain lots of the reagent cartridges show confirmed positive bias...

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

Class II — Potential Health HazardOngoing
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
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· Signal Medical Corporation

Recalled Item: Symmetric Total Knee Femoral Components Product Usage: Symmetric Total Knee...

The Issue: Packaging of a device was compromised

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
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· 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
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· 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
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
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
FoodSeptember 26, 2014· General Mills, Inc.

Recalled Item: Cases of Pillsbury Biscuits Buttermilk 4pk. (6 - 4pk / case) Recalled by...

The Issue: Undeclared Milk ingredient on retail package. In error, individually wrapped...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 26, 2014· General Mills, Inc.

Recalled Item: Pillsbury Biscuit Flaky Layers retail 4pk package. Recalled by General...

The Issue: Undeclared Milk ingredient on retail package. In error, individually wrapped...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 26, 2014· Teleflex Medical

Recalled Item: Pilling Knife Handles: a) b) c) Recalled by Teleflex Medical Due to The...

The Issue: The knife handles slot depth is out of specification, so blades may not fit...

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
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 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· 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· 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