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. 2,563 recalls have been distributed to Minnesota in the last 12 months.
Showing 18061–18080 of 52,120 recalls
Recalled Item: Kit Model #65193091 Recalled by Medline Industries Inc Due to Non-sterile...
The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liberty Select Cycler Software Version 2.9.0 Model Number 180343 and...
The Issue: The device may detect an incorrect Heater Bag volume which may lead to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Hand Sanitizer Gel Recalled by Genesis Partnership Company SA Due to...
The Issue: CGMP Deviations: hand sanitizers were recalled because they were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Panagel Hand Sanitizer Recalled by Genesis Partnership Company SA Due to...
The Issue: CGMP Deviations: hand sanitizers were recalled because they were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Genesis Hand Sanitizer Gel Recalled by Genesis Partnership Company SA Due to...
The Issue: CGMP Deviations: hand sanitizers were recalled because they were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Killz Germz Hand Sanitizer Recalled by Genesis Partnership Company SA Due to...
The Issue: Sub-Potent Drug; Killz GERMz was recalled due to sub-potent results. Testing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Killz Germz Hand Sanitizer Recalled by Genesis Partnership Company SA Due to...
The Issue: Sub-Potent Drug; Killz GERMz was recalled due to sub-potent results. Testing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Synapse PACS Software Versions 5.1 and higher Recalled by Fujifilm Medical...
The Issue: There is a potential for the wrong patient information may be displayed in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bien-Air Surgery SN ******* MULTIFUNCTION PEDAL OSSEODUO - Recalled by...
The Issue: The magnet located inside the foot pedal may come off and may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bien-Air Surgery SN ******* OSSEOSTAP Footcontrol - Product Recalled by...
The Issue: The magnet located inside the foot pedal may come off and may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS Software Version 5.6.1 - Product Usage: intended for Recalled...
The Issue: FUJIFILM has become aware of the possibility that certain CT studies may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bien-Air Surgery SN **** FOOTCTRL OSSEODOC - Product Recalled by Bien-Air...
The Issue: The magnet located inside the foot pedal may come off and may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entellus Medical SN ******* Shaver System Foot Pedal Recalled by Bien-Air...
The Issue: The magnet located inside the foot pedal may come off and may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments SN ******* S2 MINI FOOT Pedal Recalled by Bien-Air...
The Issue: The magnet located inside the foot pedal may come off and may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Citalopram Oral Solution Recalled by PAI Holdings, LLC. dba Pharmaceutical...
The Issue: Failed Impurities/Degradation Specifications; high out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Microwave popcorn packaged in the following ways: 1) Full Circle Recalled by...
The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Light microwave popcorn packaged in the following ways: 1) Full Recalled by...
The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lightly salted microwave popcorn packaged in the following ways: 1) Recalled...
The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cadia Organic Unsalted Microwave Popcorn Recalled by Gilster-Mary Lee Corp....
The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Buttered microwave popcorn packaged in the following ways: 1) Full Recalled...
The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...
Recommended Action: Do not consume. Return to store for a refund or discard.