Product Recalls in Minnesota
Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,478 recalls have been distributed to Minnesota in the last 12 months.
Showing 27821–27840 of 52,120 recalls
Recalled Item: Progesterone USP (Micronized) (Yam) for prescription compounding Recalled by...
The Issue: CGMP Deviations: Lack of stability data and controls to support the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluconazole USP for prescription compounding Recalled by American...
The Issue: CGMP Deviations: Lack of stability data and controls to support the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ascorbic Acid USP Recalled by American Pharmaceutical Ingredients LLC Due to...
The Issue: CGMP Deviations: Lack of stability data and controls to support the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Itraconazole USP (Micronized) for prescription compounding Recalled by...
The Issue: CGMP Deviations: Lack of stability data and controls to support the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levocetirizine Dihydrochloride for prescription compounding Recalled by...
The Issue: CGMP Deviations: Lack of stability data and controls to support the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kratom capsules labeled in the following ways: 1) Divinity Kratom Recalled...
The Issue: The firm's dietary supplement products contain kratom (Mitragyna speciosa),...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kratom powder labeled in the following ways 1) Enhance Your Life Recalled by...
The Issue: The firm's dietary supplement products contain kratom (Mitragyna speciosa),...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: White Quinoa Recalled by InHarvest, Inc. Due to Firm was notified by...
The Issue: Firm was notified by customer that some bags of White Quinoa actually...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Product packaged in the following ways A) Sonne's Recalled by Vitalab Co Inc...
The Issue: The firm's vitamin C dietary supplement contains lactose, a milk-derived...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Stanbio AC power adapter for the HemoPoint H2 meter Recalled by Stanbio...
The Issue: The US prong (type A) adapter plate may crack, break, or detach and remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE isp with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT(R) ClearVUE(R) isp with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim Implantable Port with Smooth Septum and Attachable...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE isp with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.