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. 2,673 recalls have been distributed to Minnesota in the last 12 months.
Showing 5061–5080 of 52,120 recalls
Recalled Item: Stryker iBur 4.0mm Precision Round Recalled by Stryker Corporation Due to...
The Issue: Potential for the product to exhibit temperatures higher than specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker TMJ Unilateral Implant Recalled by TMJ Solutions Inc Due to...
The Issue: Patient-fitted temporomandibular (TMJ) prothesis contained incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker iBur 3.0mm Coarse Diamond Round Recalled by Stryker Corporation Due...
The Issue: Potential for the product to exhibit temperatures higher than specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker iBur 3.0mm Precision Round Recalled by Stryker Corporation Due to...
The Issue: Potential for the product to exhibit temperatures higher than specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (a) CardinalHealth Salem Sump Dual Lumen Stomach Tube with Anti- Valve...
The Issue: The firm received reports of breakage in the Anti- Valve (ARV) due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (a) CardinalHealth Salem Sump Dual Lumen Stomach Tube Recalled by Cardinal...
The Issue: The firm received reports of breakage in the Anti- Valve (ARV) due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: regard Clinical Packaging Solutions Recalled by ROi CPS LLC Due to Medical...
The Issue: Medical convenience kits were distributed with Merit syringes (manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker iBur 5.0mm Coarse Diamond Round Recalled by Stryker Corporation Due...
The Issue: Potential for the product to exhibit temperatures higher than specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B. Braun Medical Inc Due to...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ciprofloxacin ophthalmic solution USP Recalled by FDC Limited Due to...
The Issue: Defective container: unable to get the solution out of the bottle as the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VariSoft Infusion Set Recalled by Unomedical A/S Due to Specific VariSoftTM...
The Issue: Specific VariSoftTM Infusion Sets were packaged using incorrect secondary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glenmark Recalled by Glenmark Pharmaceuticals Inc., USA Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.