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. 2,604 recalls have been distributed to Minnesota in the last 12 months.
Showing 12581–12600 of 52,120 recalls
Recalled Item: Zonisamide Capsules USP Recalled by Direct Rx Due to CGMP Deviations: Gaps...
The Issue: CGMP Deviations: Gaps in the quality system in the Quality Control...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RayOne Preloaded Hydrophilic Acrylic IOL Injection Systems containing one...
The Issue: The outer package is mislabeled and the package contains a different IOL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EEA Autosuture Circular Stapler with DST Series Technology Recalled by...
The Issue: The affected staplers have the potential for the staple guide to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Visions PV. 035 Digital IVUS Catheter Recalled by Volcano Corp Due...
The Issue: Digital IVUS catheter instructions for use ( IFU) do not contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Visions PV. 035 Digital IVUS Catheter Recalled by Volcano Corp Due...
The Issue: Digital IVUS catheter instructions for use ( IFU) do not contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anagrelide Capsules USP Recalled by Teva Pharmaceuticals USA Inc Due to...
The Issue: Failed Dissolution Specifications- Low Out-Of-Specification results obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wise Woman Herbals Standardized Kava Glycerite Recalled by EarthLab Inc Due...
The Issue: The microbial test result is found to be out of specification due to high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wise Woman Herbals Sleepytime Glycerite. Product is liquid and strength...
The Issue: The microbial test result is found to be out of specification due to high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wise Woman Herbals Kava Capsules Recalled by EarthLab Inc Due to The...
The Issue: The microbial test result is found to be out of specification due to high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Butter Buds Food Ingredients. Butter Buds 8X Non-Dairy LD Recalled by Butter...
The Issue: Undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wisco Pop Strawberry Soda Recalled by Karben4 Brewing LLC Due to Cans of...
The Issue: Cans of soda may contain yeast.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wisco Pop Cherry Soda Recalled by Karben4 Brewing LLC Due to Cans of soda...
The Issue: Cans of soda may contain yeast.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wisco Pop Grapefruit Soda Recalled by Karben4 Brewing LLC Due to Cans of...
The Issue: Cans of soda may contain yeast.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wisco Pop Ginger Soda Recalled by Karben4 Brewing LLC Due to Cans of soda...
The Issue: Cans of soda may contain yeast.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medline Pill Splitters Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Product lid (which houses a blade) is coming unhinged from the base, thus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premium Nature Instant Hand Sanitizer Recalled by AMS Packaging Inc Due to...
The Issue: Subpotent Drug: FDA analysis has revealed some bottles of these products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xiidra (lifitegrast ophthalmic solution) 5% PROFESSIONAL SAMPLE Recalled by...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xiidra (lifitegrast ophthalmic solution) 5% PROFESSIONAL SAMPLE Recalled by...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xiidra (lifitegrast ophthalmic solution) 5% Recalled by Novartis...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xiidra (lifitegrast ophthalmic solution) Recalled by Novartis...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.