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. 2,561 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,561 in last 12 months

Showing 3396133980 of 55,415 recalls

DrugDecember 20, 2016· Mylan LLC.

Recalled Item: Temozolomide Capsules Recalled by Mylan LLC. Due to Failed Tablet/Capsule...

The Issue: Failed Tablet/Capsule Specifications: customer complaints of broken or...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2016· Mylan LLC.

Recalled Item: Temozolomide Capsules Recalled by Mylan LLC. Due to Failed Tablet/Capsule...

The Issue: Failed Tablet/Capsule Specifications: customer complaints of broken or...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: buPROPion Hydrochloride Extended-release Tablets Recalled by Sun...

The Issue: Failed Dissolution Specifications; 18 month stability time point

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

Class III — Low RiskOngoing
Refund
DrugDecember 19, 2016· Apotex Inc.

Recalled Item: Aripiprazole Tablets Recalled by Apotex Inc. Due to Superpotent Drug:...

The Issue: Superpotent Drug: Product may not meet specifications throughout shelf life.

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

Class III — Low RiskOngoing
Refund
FoodDecember 19, 2016· Subco Foods of Wisconsin, Inc.

Recalled Item: Best Choice French Vanilla Instant Pudding & Pie Filling Recalled by Subco...

The Issue: Subco Foods of Wisconsin was notified by their supplier that the high heat...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 19, 2016· Subco Foods of Wisconsin, Inc.

Recalled Item: Bakers Corner Vanilla Instant Pudding & Pie Filling Recalled by Subco Foods...

The Issue: Subco Foods of Wisconsin was notified by their supplier that the high heat...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 19, 2016· Subco Foods of Wisconsin, Inc.

Recalled Item: Best Choice Lemon Instant Pudding & Pie Filling Recalled by Subco Foods of...

The Issue: Subco Foods of Wisconsin was notified by their supplier that the high heat...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 19, 2016· Subco Foods of Wisconsin, Inc.

Recalled Item: Best Choice Pistachio Instant Pudding & Pie Filling Recalled by Subco Foods...

The Issue: Subco Foods of Wisconsin was notified by their supplier, that the high heat...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 19, 2016· Pinnacle Foods

Recalled Item: Buffalo Blue Kettle Cooked Potato Chips 8 oz (227g) Recalled by Pinnacle...

The Issue: Snyder of Berlin is recalling their Buffalo Blue Kettle Cooked Potato Chips...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 19, 2016· Beckman Coulter Inc.

Recalled Item: DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter Inc....

The Issue: Beckman Coulter has determined that additional clarification for the Blast...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2016· Beckman Coulter Inc.

Recalled Item: UniCel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Beckman Coulter has determined that additional clarification for the Blast...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2016· GE OEC Medical Systems, Inc

Recalled Item: The OEC 9900 Elite mobile fluoroscopy system is designed to Recalled by GE...

The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2016· Zimmer Biomet, Inc.

Recalled Item: Active Articulation ArComXL Polyethylene Bearings Active Articulation...

The Issue: Product complaints indicated that the part and lot numbers on the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2016· Bard Access Systems

Recalled Item: SafeStep¿ Huber Needle Set with Y-Injection Site. Product Code: LH-0029YN....

The Issue: Bard Access Systems announces a voluntary field action for the SafeStep¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2016· Zimmer Biomet, Inc.

Recalled Item: RingLoc ArComXL Highly Crosslinked Polyethylene Liners ArComXL High Wall...

The Issue: Product complaints indicated that the part and lot numbers on the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2016· Bard Access Systems

Recalled Item: MiniLoc¿ Safety Infusion Set Winged without Y-Injection Site. Product Code:...

The Issue: Bard Access Systems announces a voluntary field action for the SafeStep¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2016· GE OEC Medical Systems, Inc

Recalled Item: OEC MiniView 6800. MDL Number: D002533 The OEC MiniView 6800 Recalled by GE...

The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2016· GE OEC Medical Systems, Inc

Recalled Item: OEC 9800. MDL Numbers: D222250 Recalled by GE OEC Medical Systems, Inc Due...

The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: IQon Spectral CT with software version 4.7.0 Product Usage: The Recalled by...

The Issue: Multiple issues have caused the device to result in CT rescans or incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2016· DICOM GRID INC

Recalled Item: Ambra PACS UDI: +AMBRHEALTHSOLUTIONS0/$$+7_V3.16.13.0R Software Version...

The Issue: A software error caused the window/level to become the same in one series...

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

Class II — Potential Health HazardOngoing