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. 1,075 recalls have been distributed to Minnesota in the last 12 months.
Showing 16521–16540 of 52,120 recalls
Recalled Item: Cefprozil for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thumbs Up 7 Red 70K Recalled by Antoto-K Due to Marketed without Approved...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Imperial Extreme 2000 Capsules Recalled by S & B Story LLC Due to Marketed...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PremierZen Black 5000 capsules Recalled by Namoo Enterprise LLC Due to...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mometasone Furoate Topical Solution Recalled by Cosette Pharmaceuticals,...
The Issue: CGMP Deviaitons
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin HCl Extended-Release Tablets Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Moisture Limits: Out of specification for water content
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZVplasty Directional Cement Cannula Long Recalled by Zavation Due to...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InterV 10G Bone Access Tools/Kit Recalled by Zavation Due to Products...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty Direct Bipedicular Bone Access Kit with Drill Recalled by Zavation...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 G Coxaxial Cannula with Tuohy Connection Recalled by Zavation Due to...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 GAUGE DIRECT UNILATERAL STYLET(1 X DIAMOND 1 X BEVEL) Recalled by...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10G BEVELED TROCAR/CANNULA. For use in Orthopedic / spinal procedures....
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CEMIX - CEMENT MIXING SYSTEM STERILE Recalled by Zavation Due to Products...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty Cement Delivery Cannula Recalled by Zavation Due to Products...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty Recalled by Zavation Due to Products distributed as sterile may not...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty Biopsy Device Recalled by Zavation Due to Products distributed as...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11G DIRECT DOUBLE BONE ACCESS KIT. For use in Orthopedic / spinal...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVPlasty Recalled by Zavation Due to Products distributed as sterile may not...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty Recalled by Zavation Due to Products distributed as sterile may not...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty 10G Recalled by Zavation Due to Products distributed as sterile may...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.