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. 1,749 recalls have been distributed to Minnesota in the last 12 months.
Showing 46801–46820 of 52,120 recalls
Recalled Item: Acetaminophen Tablets Recalled by Marlex Pharmaceuticals, Inc. Due to CGMP...
The Issue: CGMP Deviations: The recalled acetaminophen tablet lot was not manufactured...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tekturna HCT (aliskiren and hydrochlorothiazide) Tablets 150/12.5 mg...
The Issue: Chemical Contamination: Novartis Pharmaceuticals Corporation has recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diovan (valsartan) 160 mg per tablet Recalled by Novartis Pharmaceuticals...
The Issue: Chemical Contamination: Novartis Pharmaceuticals Corporation has recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Exforge HCT (amlodipine Recalled by Novartis Pharmaceuticals Corp. Due to...
The Issue: Chemical Contamination: Novartis Pharmaceuticals Corporation has recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Exforge HCT (amlodipine Recalled by Novartis Pharmaceuticals Corp. Due to...
The Issue: Chemical Contamination: Novartis Pharmaceuticals Corporation has recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips Easy Upgrade DR Recalled by Philips Healthcare Inc. Due to The...
The Issue: The mirror icon on the bottom of each image could be misinterpreted as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon 24 Large Titanium Clips with Adhesive Backing Recalled by Teleflex...
The Issue: The manufacturing and expiration dates are not printed on the blister pack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Introvale (levonorgestrel and ethinyl estradiol) tablets Recalled by Sandoz...
The Issue: Contraceptive tablets out of sequence: Contraceptive tablets out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enhancement Medical expression. model # EXP-150. Injectable Gel 1.5cc...
The Issue: Manufacturer made a change in the production process that resulted in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E-Z Clean¿ Disposable Laparoscopic Electrode Model Number 0100L and 0100LS....
The Issue: Megadyne Medical Products is recalling certain lots of E-Z Clean, L-Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips MR Systems: Asset 0.5T Recalled by Philips Medical Systems...
The Issue: There is a potential for water to collect in the vent pipe elbow in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Ultrasound ViewPoint 6. Product Usage: ViewPoint is intended to Recalled...
The Issue: GE has recently become aware of a potential safety issue due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX Ultra 6.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX Ultra HA 6.5 mm with 2 ULTRABRAID Suture Recalled by Smith & Nephew,...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIORAPTOR 2.9 mm Suture Anchor with DURABRAID" Suture Recalled by Smith &...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX Ultra HA 4.5 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX Ultra PLLA/HA 6.5 mm with 3 ULTRABRAID Suture Recalled by Smith &...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIORAPTOR 2.9 mm Suture Anchor Recalled by Smith & Nephew, Inc. Endoscopy...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID Suture Recalled by Smith &...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEORAPTOR 2.3 mm with 1 ULTRABRAID Suture Recalled by Smith & Nephew, Inc....
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.