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 27721–27740 of 52,120 recalls
Recalled Item: Intra-Aortic Balloon Catheter Mega 7.5FR 40cc Product Usage: The...
The Issue: The U.S. Instructions For Use for the Mega Intra-Aortic Balloon (IAB)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 with 4.1.7 XX026 software version model number 728231 Recalled...
The Issue: Surview scan with tube current lower than 30 mA is unable to be initialized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intra-Aortic Balloon Catheter Mega 8FR 50cc Product Usage: The intra-aortic...
The Issue: The U.S. Instructions For Use for the Mega Intra-Aortic Balloon (IAB)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Acute Care System (IACS) Monitoring Solution Recalled by Draegar...
The Issue: The invasive pressure visual and audible alarms may not activate.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: F-T3SYSTEM Recalled by Allen Medical Systems Due to The recalling firm has...
The Issue: The recalling firm has become aware that the rail section clamps used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Labetalol Hydrochloride Injection Recalled by Hospira Inc. A Pfizer Company...
The Issue: Defective Container: Cracked glass at the rim surface of glass vials,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lotte Kancho Choco-Biscuit Recalled by Lotte International America Corp. Due...
The Issue: Firm was notified by customer of peanut allergen found in the product during...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Presource PBDS Recalled by Cardinal Health 200, LLC Due to A defect in the...
The Issue: A defect in the seal of the Gatorade pouch contained in kits caused the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource PBDS Recalled by Cardinal Health 200, LLC Due to A defect in the...
The Issue: A defect in the seal of the Gatorade pouch contained in kits caused the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource PBDS Recalled by Cardinal Health 200, LLC Due to A defect in the...
The Issue: A defect in the seal of the Gatorade pouch contained in kits caused the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource PBDS Recalled by Cardinal Health 200, LLC Due to A defect in the...
The Issue: A defect in the seal of the Gatorade pouch contained in kits caused the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza software VB10A model numbers: 10863171 Recalled by Siemens...
The Issue: Software upgrade to correct format of study dates and issues with Legacy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza software Syngo.Plaza is a Picture Archiving and Communication...
The Issue: Software upgrade to correct format of study dates and issues with Legacy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EBI Osteogen Implantable Bone Growth Stimulator The OsteoGen Implantable...
The Issue: Lack of adequate validation and controls to ensure that product cleanliness...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpF PLUS-Mini (60 ¿A/W) Implantable Spinal Fusion Stimulator SpF PLUS-Mini...
The Issue: Lack of adequate validation and controls to ensure that product cleanliness...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Irrigation USP Recalled by B. Braun Medical Inc Due to...
The Issue: Presence of Particulate Matter: Customer complaint of particulate matter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Strauss Penis Clamp 130MM/General Instruments Recalled by Aesculap Implant...
The Issue: The plastic sleeves of the Penis Clamp and Mouth Gag may stick together...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Doyen-Collin Mouth Gag 120MM/ General Instruments Recalled by Aesculap...
The Issue: The plastic sleeves of the Penis Clamp and Mouth Gag may stick together...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PVP Scrub Solution Recalled by Medline Industries Inc Due to Subpotent Drug:...
The Issue: Subpotent Drug: product not meeting the iodine assay level requirements...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Seggiano Artichoke & Garlic Sauce & Spread Net Weight 200g Recalled by...
The Issue: The Tuscan Kale Pesto was mislabeled as Seggiano Artichoke & Garlic Sauce &...
Recommended Action: Do not consume. Return to store for a refund or discard.