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. 2,478 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,478 in last 12 months

Showing 2872128740 of 52,120 recalls

FoodOctober 16, 2017· Midway Specialty Vehicles LLC

Recalled Item: Triple Chocolate Mudslide Cookie Recalled by Midway Specialty Vehicles LLC...

The Issue: Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 16, 2017· Midway Specialty Vehicles LLC

Recalled Item: Oatmeal Cookie Recalled by Midway Specialty Vehicles LLC Due to Undeclared...

The Issue: Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 16, 2017· Midway Specialty Vehicles LLC

Recalled Item: M&M Cookie Recalled by Midway Specialty Vehicles LLC Due to Undeclared Peanut

The Issue: Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 16, 2017· Midway Specialty Vehicles LLC

Recalled Item: Snickerdoodle Cookie Recalled by Midway Specialty Vehicles LLC Due to...

The Issue: Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 16, 2017· Midway Specialty Vehicles LLC

Recalled Item: Chocolate Chip-N-Chunk Cookie Recalled by Midway Specialty Vehicles LLC Due...

The Issue: Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 16, 2017· Midway Specialty Vehicles LLC

Recalled Item: Red Velvet Cookie Recalled by Midway Specialty Vehicles LLC Due to...

The Issue: Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 16, 2017· Midway Specialty Vehicles LLC

Recalled Item: Amish Sugar Cookie Recalled by Midway Specialty Vehicles LLC Due to...

The Issue: Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 16, 2017· Midway Specialty Vehicles LLC

Recalled Item: Iced Sugar Frosted Cookie Recalled by Midway Specialty Vehicles LLC Due to...

The Issue: Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 16, 2017· Midway Specialty Vehicles LLC

Recalled Item: Frosted Brownie Cookie Recalled by Midway Specialty Vehicles LLC Due to...

The Issue: Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 16, 2017· C.R. Bard, Inc.

Recalled Item: Medivance ArcticGel Small Pad Kit - a box containing a single foil pouch...

The Issue: Hydrogel peeling from the pads.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2017· Fukuda Denshi Co., Ltd.

Recalled Item: Fukuda Denshi patient monitor model DS-8100M and DS-8100N Product Usage:...

The Issue: For the Fukuda Denshi patient monitor model DS-8100, in less than 0.003%...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2017· DeRoyal Industries Inc

Recalled Item: DeRoyal Sterile Custom kits containing Medline Aplicare Povidone Iodine Prep...

The Issue: Custom surgical kits contain Aplicare Povidone Iodine Prep Pads which were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugOctober 13, 2017· Sanofi-Aventis U.S. LLC

Recalled Item: Clofarabine injection Recalled by Sanofi-Aventis U.S. LLC Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Package Insert: authorized generic product...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 12, 2017· Genzyme Corporation

Recalled Item: Clolar (clofarabine) 20 mg/20 mL (1 mg/mL) Injection Recalled by Genzyme...

The Issue: Labeling: Incorrect or Missing Package Insert.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodOctober 12, 2017· Slade Gorton & Company, Inc.

Recalled Item: Icybay Brand Frog Legs Recalled by Slade Gorton & Company, Inc. Due to...

The Issue: Unapproved antibiotics-Nitrofurans and Chloramphenicol present

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 11, 2017· Zimmer Biomet, Inc.

Recalled Item: TunneLoc Tibial Fixation Device (Within an ACL Kit) Product Usage: Recalled...

The Issue: Gamma sterilization validation testing indicates the sterilization dose for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· Zimmer Biomet, Inc.

Recalled Item: TunneLoc Tibial Fixation Device Product Usage: To provide fixation of...

The Issue: Gamma sterilization validation testing indicates the sterilization dose for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· GE Medical Systems China Co., Ltd.

Recalled Item: Carestation 620 A2 Recalled by GE Medical Systems China Co., Ltd. Due to...

The Issue: Possible incomplete seal between the CO2 absorber and the breathing circuit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· GE Medical Systems China Co., Ltd.

Recalled Item: Carestation 620 A1 Recalled by GE Medical Systems China Co., Ltd. Due to...

The Issue: Possible incomplete seal between the CO2 absorber and the breathing circuit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· Zimmer Dental Inc

Recalled Item: Zimmer Dental GemLock RHD2.5 Hex Driver. The label shows the Recalled by...

The Issue: The device may contain a manufacturing condition affecting the geometry of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing