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 30201–30220 of 52,120 recalls
Recalled Item: Gourmet Bay - Toasted Crumb Breaded Tilapia Recalled by Slade Gorton &...
The Issue: Products recalled due to undeclared allergen -milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: WICK'S (4) Oven-Ready Recalled by Wicks Due to Undeclared Milk
The Issue: The firm's breaded seafood products were breaded using an ingredient, which...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Code: LM290 Recalled by Wicks Due to Undeclared Milk
The Issue: The firm's breaded seafood products were breaded using an ingredient, which...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: NasalCrom (cromolyn sodium) Nasal Spray Recalled by Bausch & Lomb, Inc. Due...
The Issue: CGMP Deviations: Possibility of the presence of microbial contamination in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Helix Elite" Molecular Standards: Inactivated Standard. Inactivated...
The Issue: Real-time shelf life testing failed at 24 months
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbiologics QC Sets and Panels: Helix Elite. Extended Enteric Bacterial...
The Issue: Real-time shelf life testing failed at 24 months
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite" Molecular Standards: Inactivated Standard. Inactivated...
The Issue: Real-time shelf life testing failed at 24 months
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite" Molecular Standards: Inactivated Standard. Inactivated...
The Issue: Real-time shelf life testing failed at 24 months
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbiologics QC Sets and Panels. BD MAX" CT/GC/TV Verification and...
The Issue: Real-time shelf life testing failed at 24 months
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectranetics Turbo-Elite Laser Atherectomy Catheter Peripheral Rapid...
The Issue: Potential for flouroscopially visible marker band at the tip of the Rapid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axiom Artis Recalled by Siemens Medical Solutions USA, Inc Due to Potential...
The Issue: Potential for liquid entry
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q and Q.Zen Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for liquid entry
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Zee and Zeego Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for liquid entry
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CER OPTION TYPE 1 TPR SLEVE -6 Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COMP 12MM HUM FRAC STEM MACRO Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSS CEMENTED IM STEM 12X150 Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RED SEXP DSTL FEM 19CM LT ASSY Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RED SEXP DSTL FEM 19CM RT ASSY Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COMP PRIMARY STEM 8MM MINI Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CER BIOLOXD OPTION HD 32MM Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.