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. 2,497 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,497 in last 12 months

Showing 4240142420 of 55,415 recalls

Medical DeviceMarch 19, 2015· Biosense Webster, Inc.

Recalled Item: SMARTABLATE RF Generator System Recalled by Biosense Webster, Inc. Due to...

The Issue: Biosense Webster is recalling the SMARTABLATE Generator System because...

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

Class II — Potential Health HazardOngoing
FoodMarch 19, 2015· Giant Eagle, Inc.

Recalled Item: GetGo Giant Eagle Strawberry Yogurt Parfait Sell By: (up to Recalled by...

The Issue: Giant Eagle label review found that labels of GetGo Strawberry Yogurt...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 18, 2015· Biomet, Inc.

Recalled Item: LOW PROFILE NON-LOCK SCREW Recalled by Biomet, Inc. Due to A Biomet...

The Issue: A Biomet investigation found that the Low Profile Non-Locking Screw...

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

Class II — Potential Health HazardOngoing
DrugMarch 18, 2015· Baxter Healthcare Corp.

Recalled Item: 5% Dextrose Injection Recalled by Baxter Healthcare Corp. Due to Lack of...

The Issue: Lack of Assurance of Sterility. Complaints were receive of missing closures...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 18, 2015· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...

The Issue: Lack of Assurance of Sterility. Complaints were receive of missing closures...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 18, 2015· Mylan Institutional LLC

Recalled Item: CARBOplatin Injection 450 mg/45 mL (10 mg/mL) Recalled by Mylan...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 18, 2015· Mylan Institutional LLC

Recalled Item: Methotrexate Injection Recalled by Mylan Institutional LLC Due to Presence...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 17, 2015· Akorn, Inc.

Recalled Item: SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION Recalled by Akorn, Inc....

The Issue: Failed Dissolution Specifications: Out of specification for dissolution of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 17, 2015· Akorn, Inc.

Recalled Item: SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION Recalled by Akorn, Inc....

The Issue: Failed Dissolution Specifications: Out of specification for dissolution of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 17, 2015· Akorn, Inc.

Recalled Item: SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION Recalled by Akorn, Inc....

The Issue: Failed Dissolution Specifications: Out of specification for dissolution of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 17, 2015· Biocare Medical, LLC

Recalled Item: CD99 Catalog number PM008 AA Recalled by Biocare Medical, LLC Due to A drop...

The Issue: A drop in staining intensity over time has been observed. These lots may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Head Holder shipped with Ingenuity Core Computed Tomography X-ray Systems....

The Issue: A head holder released for use with other CT systems but not yet qualified...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Head Holder shipped with Ingenuity CT Computed Tomography X-ray Systems...

The Issue: A head holder released for use with other CT systems but not yet qualified...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2015· American Catheter Corp

Recalled Item: American Catheter / Cholangiogram Catheter 9100 Series. Recalled by American...

The Issue: Catheters were not sealed before sterilization. and was not detected through...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Head Holder shipped with Ingenuity Core 128 Computed Tomography X-ray...

The Issue: A head holder released for use with other CT systems but not yet qualified...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2015· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Dual Chamber Temporary External Pacemaker Recalled by Medtronic...

The Issue: Possible performance issue when used with specific AA-sized (LR6) batteries....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2015· Bard Peripheral Vascular Inc

Recalled Item: Bard Monopty Disposable Core Biopsy Instruments and Kits Recalled by Bard...

The Issue: Bard Peripheral Vascular is recalling the Bard Monopty Disposable Core...

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

Class II — Potential Health HazardOngoing
FoodMarch 17, 2015· Kraft Foods Group Inc.

Recalled Item: Kraft Macaroni & Cheese Boxed Dinner Original Flavor Recalled by Kraft Foods...

The Issue: This voluntary recall has been initiated because Kraft Macaroni & Cheese...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 17, 2015· Giant Eagle, Inc.

Recalled Item: All varieties and packaging configurations of cut out cookies labeled...

The Issue: Cut Out Cookies sold in Giant Eagle Bakeries were recalled due to an...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 17, 2015· Trader Joes Company

Recalled Item: Trader Joe's Nuts Raw California Walnut Pieces NET WT. 16oz. Recalled by...

The Issue: The firm is recalling Raw Walnuts because the products have the potential to...

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

Class I — Serious Health HazardOngoing
Refund