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. 1,099 recalls have been distributed to Minnesota in the last 12 months.
Showing 13961–13980 of 52,120 recalls
Recalled Item: Presidents Choice 12 oz Mixed Greens / Le Choix du Recalled by Dole Fresh...
The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Presidents Choice 12.25oz Ranch Kit / Le Choix du President Recalled by Dole...
The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Marketside 24oz Classic Salad SKU: 3193 Recalled by Dole Fresh Vegetables...
The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HEB 9.5oz Premium Ranch Kit SKU: 3349 Recalled by Dole Fresh Vegetables Inc...
The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Little Salad Bar 8 oz Shredded Lettuce SKU: 3404 Recalled by Dole Fresh...
The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ingenia 1.5T (Product Number 781396) - HA FlexTrak II (Accessory Recalled by...
The Issue: Magnetic materials were used for the wheels of trolley. Wheels with magnetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition X (Product Number 781358) - HA FlexTrak II Recalled by...
The Issue: Magnetic materials were used for the wheels of trolley. Wheels with magnetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition X (Product Number 781356) - HA FlexTrak II Recalled by...
The Issue: Magnetic materials were used for the wheels of trolley. Wheels with magnetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sufentanil Citrate Injection Recalled by Akorn, Inc. Due to Subpotent Drug:...
The Issue: Subpotent Drug: Out of specification for assay at the 30-month stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Semglee (insulin glargine) injection Recalled by Mylan Pharmaceuticals Inc...
The Issue: Labeling: Missing Label: label missing from some Semglee prefilled pens.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ATTUNE REVISION POSTERIOR FEMORAL AUGMENT SZ 9 12MM-intended as a Recalled...
The Issue: May have adhesive residue on the posterior surface of the femoral augment,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Veritor Plus Analyzer - intended to provide rapid test Recalled by Becton...
The Issue: May have the potential to overheat and/or cause fire, the issue can occur...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE REVISION DISTAL FEMORAL AUGMENT SZ 6 4MM- Intended as Recalled by...
The Issue: May have adhesive residue on the posterior surface of the femoral augment,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRA SURFIX ALPHA Screwdriver Torx 10 Recalled by Smith & Nephew, Inc....
The Issue: The affected screwdrivers are out of specification and may not mate with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Optima Coil System consists of an implantable embolization coil Recalled...
The Issue: Due to Label/Pouch mix-up. Pouches incorrectly labeled. Incorrect shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leader Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QC QUALITY CHOICE Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CVS Health Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: equate Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rugby Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.