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. 2,609 recalls have been distributed to Michigan in the last 12 months.
Showing 21701–21720 of 53,342 recalls
Recalled Item: Glazed Pumpkin Cake Donut Recalled by WESTON FOODS (CANADA) INC Due to...
The Issue: Product contains lead and other pieces of metal sized .5mm -2.0mm.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pumpkin Cake Roll - Pumpkin Spice Cake Roll with Creme Recalled by WESTON...
The Issue: Product contains lead and other pieces of metal sized .5mm -2.0mm.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Xhibit Central Recalled by Spacelabs Healthcare, Inc. Due to The firm...
The Issue: The firm received reports of loss of audio alarm after a power failure or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transducer S8-3t UDI (01)00884838073524 Can be used as Recalled by Philips...
The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transducer S7-3t UDI (01)00884838061439 Can be used with: Recalled by...
The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transducer S8-3t UDI (01)00884838067523 Can be used with: Recalled by...
The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transducer S7-3t UDI (01)00884838067530 Used as accessory with: Recalled by...
The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPROTTE Lumbar with Introducer Recalled by Pajunk GmbH Due to Problem with...
The Issue: Problem with packaging sealing process which affects sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ApexPro Telemetry Server System. Also identified as Modification To: ApexPro...
The Issue: May not provide visual and/or audible alarms at the CARESCAPE Central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fentanyl Citrate Active Pharmaceutical Ingredient Recalled by Johnson...
The Issue: cGMP Deviations: Potential glass contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cisplatin Active Pharmaceutical Ingredient Recalled by Johnson Matthey Inc....
The Issue: cGMP Deviations: Potential glass contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxaliplatin Active Pharmaceutical Ingredient Recalled by Johnson Matthey...
The Issue: cGMP Deviations: Potential glass contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dario Blood Glucose Monitoring System Recalled by LABSTYLE INNOVATIONS Due...
The Issue: The Dario-Blood Glucose Tracker Android App versions 4.3.0-4.3.2 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVKARE Fexofenadine Hydrochloride Tablets USP Antihistamine 180 mg Recalled...
The Issue: Failed Stability Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Plastic Bottles labeled with: "Ancient Youth Secret - Since 500 B.C....
The Issue: Product label declares Vitamin D3 at 200 IU per serving. FDA sample analysis...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Centurion CIRCLAMP W/1.3 CM BELL-single-use Recalled by Centurion Medical...
The Issue: A mismatch between the angle of the hole in the base and the angle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas c 701 and 702 Analyzer/Module-RF interference claims for the Recalled...
The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion CIRCLAMP W/1.1CM BELL - single-use Recalled by Centurion Medical...
The Issue: A mismatch between the angle of the hole in the base and the angle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas c 311 Recalled by Roche Diagnostics Operations, Inc. Due to Tina-quant...
The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lamivudine Tablets Recalled by American Health Packaging Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Package Insert; an error in the Dosage Forms...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.