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 29881–29900 of 52,120 recalls
Recalled Item: Succinylcholine Chloride Recalled by Fagron Compounding Services LLC dba...
The Issue: Lack Of Assurance Of Sterility: voluntary recall initiated by the commercial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LANTANA White Bean HUMMUS NET WT. 10 oz (283g) Recalled by House Of Thaller...
The Issue: The firm was notified by their ingredient supplier that the pine nuts may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Marketside CLASSIC HUMMUS WITH PINE NUTS NET WT. 10 oz (283g) Recalled by...
The Issue: The firm was notified by their ingredient supplier that the pine nuts may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FRESH FOODS MARKET Artisan Humus Pine Nuts NET WT 10 oz (283g) Recalled by...
The Issue: The firm was notified by their ingredient supplier that the pine nuts may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CS 100i Intra-Aortic Balloon Pump Recalled by Maquet Datascope Corp -...
The Issue: The device failed to pump due to an electrical test failure code #58 (power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 100 Intra-Aortic Balloon Pump Recalled by Maquet Datascope Corp - Cardiac...
The Issue: The device failed to pump due to an electrical test failure code #58 (power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Max Implant System - Bone Tap for use with 7.0mm diameter Max Implant...
The Issue: An 8mm diameter bone tap was laser marked as 7mm diameter and was packed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 300 Intra-Aortic Balloon Pump Recalled by Maquet Datascope Corp - Cardiac...
The Issue: The device failed to pump due to an electrical test failure code #58 (power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Planetary Herbals Ginseng Classic Recalled by Threshold Enterprises Ltd Due...
The Issue: Product was inadvertently released prior to release of all QC testing....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clindamycin Injection USP Recalled by Alvogen, Inc Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clindamycin Injection USP Recalled by Alvogen, Inc Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ibuprofen Tablets Recalled by Time-Cap Laboratories, Inc. Due to Presence of...
The Issue: Presence of foreign tablets/capsules: Ibuprofen Tablets USP, 600 mg bottles...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clindamycin Injection USP Recalled by Alvogen, Inc Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate Oral Solution Recalled by Tris Pharma Inc. Due to Defective...
The Issue: Defective container: Oral solution leaking from container.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vis-U-All High Temperature Tubing 6"x100'. One roll per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various custom surgical kits manufactured for CMS Recalled by Custom...
The Issue: The firm manufactured and distributed custom surgical kits which contained...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum 360 Infusion System Recalled by ICU Medical Inc Due to Potential for...
The Issue: Potential for the Connectivity Engine Module of the affected unit to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 4"x11" Self Seal Pouch 200 pouches per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 3.5"x22" Self Seal Pouch 200 pouches per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 13"x18" Self Seal Pouch 100 pouches per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.