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. 2,584 recalls have been distributed to Minnesota in the last 12 months.
Showing 15861–15880 of 52,120 recalls
Recalled Item: Living Free Nerve & Muscle Plus Cetyl-Myristoleate Herbal and Glandular...
The Issue: Label declares lecithin but does not declare soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Living Free Immune Dietary Supplement Recalled by Bea Lydeckers Naturals Inc...
The Issue: Label declares lecithin but does not declare soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Living Free Nerve & Muscle Herbal Dietary Supplement Recalled by Bea...
The Issue: Label declares lecithin but does not declare soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Living Free "Adult Extra" multi-vitamin Recalled by Bea Lydeckers Naturals...
The Issue: Label declares lecithin but does not declare soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Living Free Lung & Joint Congestion Herbal Dietary Supplement Recalled by...
The Issue: Label declares lecithin but does not declare soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Living Free Heart/Blood Vessel Dietary Supplement Recalled by Bea Lydeckers...
The Issue: Label declares lecithin but does not declare soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: muRata Vios Monitoring System Model 2050 Recalled by Murata Vios, Inc. Due...
The Issue: During the set-up and workflow to begin Vios monitoring, it has been noticed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Configura Advance Chair Recalled by Accora Inc Due to The firm has...
The Issue: The firm has identified a potential for the backrest to become detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO DELTA Self Safe Recalled by Delta Med SpA Due to Problems related to the...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO DELTA Self Safe 1 Recalled by Delta Med SpA Due to Problems related to...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO DELTA SELFSAFE PUR T Recalled by Delta Med SpA Due to Problems related...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO DELTA Self Safe T Recalled by Delta Med SpA Due to Problems related to...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELTAVEN Y DNL Safety I.V. Catheter in Pur with closed Recalled by Delta Med...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO DELTA SELFSAFE PUR T Recalled by Delta Med SpA Due to Problems related...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WOLF-PAK Self Safe Safety IV Catheter: a) b) Recalled by Delta Med SpA Due...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELTAVEN Safety I.V. Catheter in Pur with closed system: a) Recalled by...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELTAVEN FASTFLASH Recalled by Delta Med SpA Due to Problems related to the...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO DELTA SELFSAFE PUR 1 Recalled by Delta Med SpA Due to Problems related...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELTAVEN Y Recalled by Delta Med SpA Due to Problems related to the...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Topotecan Injection 4 mg/4mL (1 mg/mL) Recalled by Teva Pharmaceuticals USA...
The Issue: Presence of Particulate Matter: Complaint received of a glass particle...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.