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. 2,621 recalls have been distributed to Minnesota in the last 12 months.
Showing 11901–11920 of 52,120 recalls
Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...
The Issue: Distributed VTM outside of VTM Guidance and without clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...
The Issue: Distributed VTM outside of VTM Guidance and without clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...
The Issue: Distributed VTM outside of VTM Guidance and without clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tacrolimus Ointment Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: Defective Container: Tube split from side seam
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ativan Injection (lorazepam injection Recalled by Hikma Pharmaceuticals USA...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SafeControl handset (a component of the Sentida bed which moves Recalled by...
The Issue: When the handset is disconnected from the power mains, and mains operation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuRx Diaphragm Pacing System (NeuRx DPS) External Pulse Generator (EPG)...
The Issue: Due to a defect identified on the EPG controller printed circuit board...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTERA 3000 Hepatic Artery Infusion Pump Recalled by Intera Oncology, Inc....
The Issue: Higher than expected flow rate.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentacam AXL Recalled by Oculus Optikgeraete GMBH Due to Due to a software...
The Issue: Due to a software issue, IOL calculator printout often does not accurately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentacam AXL Wave . Used to image the anterior segment of the eye. Recalled...
The Issue: Due to a software issue, IOL calculator printout often does not accurately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentacam HR . Used to image the anterior segment of the eye. Recalled by...
The Issue: Due to a software issue, IOL calculator printout often does not accurately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aripiprazole Tablets Recalled by Apotex Corp. Due to Failed dissolution...
The Issue: Failed dissolution specifications: OOS for dissolution at the 12-month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ShockPulse-SE Lithotripsy Generator Model/Serial: SPL-S Recalled by Olympus...
The Issue: Mis-wired component-the improperly wired component can result in additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Item 34033-12 Recalled by Chuckanut Bay Foods LLC Due to Undeclared Soy
The Issue: Undeclared Soy Lecithin. Label declares Chocolate Compound (Sunflower...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item 34032-12 Recalled by Chuckanut Bay Foods LLC Due to Undeclared Soy
The Issue: Undeclared Soy Lecithin. Label declares Chocolate Compound (Sunflower...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item 34021-12 Recalled by Chuckanut Bay Foods LLC Due to Undeclared Soy
The Issue: Undeclared Soy Lecithin. Label declares Chocolate Compound (Sunflower...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item 35001-12 Recalled by Chuckanut Bay Foods LLC Due to Undeclared Soy
The Issue: Undeclared Soy Lecithin. Label declares Sunflower Lecithin instead of Soy...
Recommended Action: Do not consume. Return to store for a refund or discard.