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. 1,759 recalls have been distributed to Minnesota in the last 12 months.
Showing 41681–41700 of 52,120 recalls
Recalled Item: VisiPlugST for the Lacrimal Efficiency Test. It is also sold Recalled by...
The Issue: Moisture level may cause the VisiPlugST (or CollaSyn Plugs) to break apart,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mini Naan Eight (8) nann packaged in coated paper printed Recalled by fgf...
The Issue: The products were shipped without labels declaring the nutrition and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benzonatate Capsules Recalled by Zydus Pharmaceuticals USA Inc Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: Recall due to wet and/or leaking capsules.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dacarbazine Recalled by Hospira Inc. Due to Discoloration: Reconstituted...
The Issue: Discoloration: Reconstituted solution may appear pink instead of colorless...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clinimix E 4.25/10 sulfite-free (4.25% Amino Acid with Electrolytes in...
The Issue: Lack of Assurance of Sterility; leaks were observed from the bag seam and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vintage Pure Bee Flower Honey Recalled by Vintage Food Corp. Due to Product...
The Issue: Product contains higher than recommended levels of sulfamethazine.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DRX-Revolution Mobile X-Ray System Recalled by Carestream Health Inc Due to...
The Issue: While servicing a unit at a customer site, a field engineer discovered a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer PERSONA Tibial Articular Surface Inserter Recalled by Zimmer, Inc....
The Issue: Potential for fracture of the tip of the product. The fractured tip is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TactiSys Quartz Pack Recalled by St Jude Medical Due to A configuration...
The Issue: A configuration update needs to be done on TactiSys to appropriately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autoject E1 Fixed needle device Recalled by Owen Mumford USA, Inc. Due to...
The Issue: The syringe carrier is missing components: a damper and spring.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydrALAZINE Hydrochloride Tablets Recalled by Par Pharmaceutical Inc. Due to...
The Issue: Presence of Foreign Substance: Par Pharmaceutical, Inc. is recalling one lot...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Arthrosurface HHXL (OVO) 15.6x32mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrosurface 35mm 13.5x32mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrosurface 25&30mm 10.5x28mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrosurface 25&30mm 12.5x32mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Myoglobin Calibrator (MYO CAL) Recalled by Siemens...
The Issue: Dimension Vista Myoglobin Calibrator (MYO CAL) may produce a positive shift...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Athrosurface 40mm 13.75x31mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 Recalled by...
The Issue: Needle is not captured in the needle safety sheath in specific lots.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 Recalled by...
The Issue: Needle is not captured in the needle safety sheath in specific lots.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DrugCheck Ketamine Dip Test 31317-3P PRO-EU-SWE Recalled by Express...
The Issue: This recall has been initiated due to potential false positives results when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.