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. 2,458 recalls have been distributed to Minnesota in the last 12 months.
Showing 35001–35020 of 52,120 recalls
Recalled Item: DeVilbiss Model 7305P-D Powered Suction Unit Recalled by DeVilbiss...
The Issue: A small percentage of units of 7305 Series Vacu-Aide Suction Units are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrismaSate BGK2/0 Dialysis Solution for Continuous Renal Replacement Therapy...
The Issue: Presence of leaks near top of the PrismaSate bags
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EV3 EverFiex" Self-expanding Peripheral Stent System Recalled by Ev3, Inc....
The Issue: Medtronic is issuing a medical device recall to return product potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMATE NUTRITION AMINO GOLD CAPSULES SUPER WHEY FORMULA Dietary Supplement...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Radiesse (+) Lidocaine Recalled by Merz North America, Inc. Due to...
The Issue: Complaints reported of Radiesse (+) unable to be expelled from the syringe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-wire Recalled by Integra LifeSciences Corp. Due to The affected K-wires do...
The Issue: The affected K-wires do not meet specification requirements. Specifically,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sharpoint Polypropylene Blue Monofilament 6"/15cm 9-0 USP Recalled by SSC-...
The Issue: Surgical Specialties is recalling Sharpoint Polyproplyene Blue Monofilament...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxycodone HCl Recalled by West-Ward Columbus Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specification; 9 month stability
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Doxycycline Recalled by Galderma Laboratories, L.P. Due to Labeling:...
The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: Some expiries and lot...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Product is packed in a corrugated box with poly line Recalled by Tarrier...
The Issue: The firm was notified by their supplier that the products may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Toshiba Kalare DREX-KL80 X-ray generator Recalled by Toshiba American...
The Issue: It was discovered that the generator of the system could possibly terminate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Ultimax DREX-ULT80 X-ray generator Recalled by Toshiba American...
The Issue: It was discovered that the generator of the system could possibly terminate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conical portio adapter (acorn) small & large are used for Recalled by...
The Issue: The distal end of the Conical portio adapter (acorn) is composed of a small...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammotome Revolve Dual Vacuum Assist Biopsy System Model number: MST1009...
The Issue: A 10 Gauge needle, 9cm long was shipped in an 8 Gauge needle, 15 cm package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6534-08N InterActive¿ Implant Open-Tray Transfer Narrow Part Number:...
The Issue: The incorrect sized product, InterActive Implant Open-Tray Transfer Wide,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Divalproex Sodium Delayed-release Tablets USP Recalled by Teva North America...
The Issue: Failed Tablet/Capsule Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.) Recalled...
The Issue: A version of the dual dispersive electrodes may not be compatible with some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pediatric ThermoGard¿ Dual Dispersive Electrodes (for patients 5-15 kg.)...
The Issue: A version of the dual dispersive electrodes may not be compatible with some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.