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. 1,759 recalls have been distributed to Minnesota in the last 12 months.
Showing 42601–42620 of 52,120 recalls
Recalled Item: AdVance"Male Sling System Recalled by American Medical Systems, Inc. Due to...
The Issue: During routine periodic packaging testing, AMS identified that in simulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mango flavored gelatin mix desert Recalled by U.B.C Food Distributors, LLC...
The Issue: Voluntary recall of strawberry flavored gelatin mix and mango flavored...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Saba Shark Cartilage Complex Dietary Supplement Recalled by AMS Health...
The Issue: The product is being recalled due to the potential presence of Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Strawberry flavored gelatin mix desert Recalled by U.B.C Food Distributors,...
The Issue: Voluntary recall of strawberry flavored gelatin mix and mango flavored...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hapi Pudding Recalled by J F C International Inc Due to Product's label...
The Issue: Product's label fails to declare milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sterile Water for Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose and 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lactated Ringer's and 5% Dextrose Injection Recalled by Hospira Inc. Due to...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Normosol-R pH 7.4 Multiple Electrolytes Injection Type 1 Recalled by Hospira...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection Recalled by Hospira Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lactated Ringer's Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose and 0.45% Sodium Chloride Injection Recalled by Hospira Inc. Due...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Normosol-R Multiple Electrolytes Injection Type 1 Recalled by Hospira Inc....
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.45% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Chloride in 5% Dextrose and 0.45% Sodium Chloride Injection...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Trabecular Metal Tibial Impactor. Product Usage: TM Tibial Impactor pads...
The Issue: To provide clarifying instructions relating to the assembly/disassembly of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: St Jude Medical Recalled by St Jude Medical Due to St. Jude Medical is...
The Issue: St. Jude Medical is conducting a voluntary recall of SMJ Batch # 4641580 of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM 630 Recalled by GE Healthcare, LLC Due to GE is updating the...
The Issue: GE is updating the Preventative Maintenance procedure and schedule, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM/CT 670 dual detector free-geometry integrated nuclear imaging...
The Issue: GE is issuing this recall due to a potential safety issue related to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.