Product Recalls in Michigan

Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,520 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,520 in last 12 months

Showing 3300133020 of 53,342 recalls

DrugDecember 20, 2016· Accord Healthcare, Inc.

Recalled Item: Lisinopril tablets Recalled by Accord Healthcare, Inc. Due to Failed...

The Issue: Failed tablet/capsule specification: missing break line on the 5mg tablet.

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· 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
Medical DeviceDecember 20, 2016· Zimmer Biomet, Inc.

Recalled Item: Comprehensive Reverse Shoulder System Humeral Tray Model 115340 Recalled by...

The Issue: Higher than anticipated rate of fracturing due to design. Risk of revision...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2016· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Connect Diabetes Management App Recalled by Roche Diabetes Care,...

The Issue: iOS and Android: Under certain conditions the affected app versions may...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2016· Becton Dickinson & Company

Recalled Item: Eclipse Hypodermic Needle Recalled by Becton Dickinson & Company Due to BD...

The Issue: BD is initiating a Product Advisory for the Eclipse Hypodermic Needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS Na+ Slides Recalled by Ortho-Clinical Diagnostics Due to There is a...

The Issue: There is a potential for biased results to be generated over the 10 day...

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: 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· 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· 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· 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 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 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· 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
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