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. 1,752 recalls have been distributed to Minnesota in the last 12 months.
Showing 44041–44060 of 52,120 recalls
Recalled Item: Vitamin C (ascorbic acid) Injection Recalled by Flawless Beauty LLC Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Parenteral product is sold over the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Saluta (reduced glutathione) Powder for Injection Recalled by Flawless...
The Issue: Marketed Without An Approved NDA/ANDA: Parenteral product is labeled for use...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Laroscorbine Platinium (vitamin C/collagen) injectable I.V. solution...
The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tatiomax (reduced glutathione/hydrolyzed collagen) powder for injection...
The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Water for Injection Recalled by Flawless Beauty LLC Due to Marketed...
The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips/Children's Medical Ventures Smart Monitor 2 Professional Series...
The Issue: The battery pack wire harness is improperly assembled rendering the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes ProDisc-C 2.0mm Milling Bit Recalled by Synthes, Inc. Due to Certain...
The Issue: Certain lots of the ProDisc-C 2.0mm Milling Bits have an increased potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convatec Flexi Seal Control Fecal Management System Rx Only by Convatec Inc....
The Issue: Convatec Inc. is recalling Flexi-seal FMS Control Kit since it does not have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coaxial Micro-Introducer Kit. Greatbatch Part Number/Bard Access Systems...
The Issue: Greatbatch identified that the documentation does not support the five-year...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Express Dry Seal Chest Drain ATS Blood Recovery Recalled by Atrium...
The Issue: Product that was previously recalled because the Chest Drain tubing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...
The Issue: Connection issues between the PD transfer set catheter connector and an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PediaCare brand NIGHTTIME MULTI-SYMPTOM Cold Recalled by Prestige Brands...
The Issue: Presence of Precipitate; small amounts of diphenhydramine precipitated out...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PediaCare brand DAY & NIGHT Value Pack DAYTIME MULTI-SYMPTOM Cold Recalled...
The Issue: Presence of Precipitate; small amounts of diphenhydramine precipitated out...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oasis Coil Extension Cable used with Hitachi Oasis MRI System Recalled by...
The Issue: The firm received a complaint stating the Coil Extension Cable accessory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BG3515-5 US 5mL BioGlue Surgical Adhesive. BioGlue Surgical Adhesive...
The Issue: Serum albumin component monomer failed to meet internally established end of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation software version 4.0.3.4 RayStation is a software system designed...
The Issue: This notice concerns a problem with the computation of ROI voxel volumes for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revision K Actuator Test Boards sold as replacement parts for Recalled by...
The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008T Hemodialysis Machine with Revision K Actuator Test Boards...
The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Composix" LIP Mesh with Echo PS" 7"x9" Reorder Number: Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Composix" LP with Echo PS" 10x13 HUXH0294 HUXL0314 Indicated for Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.