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.
Showing 29121–29140 of 52,120 recalls
Recalled Item: Toothette Oral Care Suction Swabs with Perox-A-Mint solution and Mouth...
The Issue: Cross Contamination With Other Products: Oral care solutions were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Toothette Oral Care Suction Toothbrush with Antiseptic Oral Rinse. Contains...
The Issue: Cross Contamination With Other Products: Oral care solutions were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Q.Care Oral Cleansing & Suctioning System Suction Toothbrush Compatible with...
The Issue: Cross Contamination With Other Products: Oral care solutions were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levophed (norepinephrine bitartrate) injection Recalled by Pfizer Inc. Due...
The Issue: Lack of sterility assurance: resulting from use of a damaged sterilizing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medfusion Recalled by Smiths Medical ASD Inc. Due to Potential for the...
The Issue: Potential for the syringe barrel clamp mechanism to loosen, decreasing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Recalled by Smiths Medical ASD Inc. Due to Potential for the...
The Issue: Potential for the syringe barrel clamp mechanism to loosen, decreasing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziptight Ankle Syndesmosis Fixation Device Recalled by Zimmer Biomet, Inc....
The Issue: Ziptight Ankle Syndesmosis Fixation was packaged without the tip protectors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUIOS CL Flow Cytometer System The AQUIOS CL Flow Cytometer Recalled by...
The Issue: Beckman Coulter has identified that an incorrect setting using a proprietary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TCC-EZ Recalled by Integra LifeSciences Corp. Due to A quarantined lot of...
The Issue: A quarantined lot of the devices was released for sale. Devices from this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A20975A "Working insert Recalled by Olympus Corporation of the Americas Due...
The Issue: Olympus has received complaints about fragments of adhesive which detached...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xper Flex Cardio Physiomonitoring system. Used to facilitate invasive...
The Issue: Intermittent communication between the host system and the FlexCardio
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza Picture Archiving and Communication System (PACS) with software...
The Issue: Software update to correct several issues that include (1)Potential data...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 3 M12 Recalled by Philips Electronics North America Corporation Due...
The Issue: When using the downscale option with the Allura R9 system or Azurion R1.1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Paroxetine tablets USP Recalled by Zydus Pharmaceuticals USA Inc Due to...
The Issue: Presence of Foreign tablets/capsules: risperidone Tablets were found in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All Sterile Products within expiry Recalled by Vital Rx, Inc. dba Atlantic...
The Issue: Lack of Assurance of Sterility .
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrocodone Bitartrate and Acetaminophen Oral Solution 7.5 mg/325 mg per...
The Issue: Labeling: Not Elsewhere Classified; product is incorrectly labeled as Class...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Honest Kids Juice Slushy Blueberry Punch Recalled by The Coca-Cola Company...
The Issue: Due to a potential package design issue, there is the possibility for...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fluorescein Sodium Recalled by Bella Pharmaceuticals, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: L-Glutamine 100mg Recalled by Bella Pharmaceuticals, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylcobalamin 10mg Recalled by Bella Pharmaceuticals, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.