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. 2,439 recalls have been distributed to Minnesota in the last 12 months.
Showing 37081–37100 of 52,120 recalls
Recalled Item: BARDEX I.C. Anti-Infective 2-Way Red Latex Foley Catheter Recalled by C.R....
The Issue: Labeling error: Catalog contains Instructions for Use (IFU) error; incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Life-Line DOCUSATE CALCIUM Sodium Free STOOL SOFTENER 240 mg each Recalled...
The Issue: Labeling: Label mix-up. Docusate Sodium 100mg Softgels were mislabeled as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VP-CH-PNV PRENATAL/POSTNATAL Prescription Folic Acid-Containing Dietary...
The Issue: Defective Delivery System: Product may contain leaking capsules.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution Recalled by Bio-pharm, Inc. Due...
The Issue: Failed Impurities/Degradation Specifications: Product recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Arthrex IBalance TKA Tibial Tray Size 2 - Catalog # AR-503-TTTC Recalled by...
The Issue: Devices reported to have a smooth texture to the outer surface of the metal,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadSuite Recalled by Merge Healthcare, Inc. Due to Potential incorrect...
The Issue: Potential incorrect Standardized Uptake Values (SUV) measurements in RadSuite.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView are gamma cameras Recalled by Philips Medical Systems (Cleveland)...
The Issue: The firm discovered four issues with the BrightView Family systems. Issue 1:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT & BrightView XCT Upgrade Recalled by Philips Medical Systems...
The Issue: The firm discovered four issues with the BrightView Family systems. Issue 1:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Stryker Color Cuff and Color Cuff II Adult Tourniquet Recalled...
The Issue: Reprocessed Stryker Pressure Tourniquet Cuffs were mislabeled, including...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X are gamma cameras Recalled by Philips Medical Systems...
The Issue: The firm discovered four issues with the BrightView Family systems. Issue 1:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dove Chocolate Assortment Snowflakes Net. Wt. 24.0 oz. Distributed by...
The Issue: Dove Chocolate Assortment Snowflakes may contain undeclared peanuts, what...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cardiosave Hybrid and rescue IABP Recalled by Maquet Datascope Corp -...
The Issue: Maquet has recieved information that in some Cardiosave IABPS, the scroll...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Inspection Technologies Recalled by GE Inspection Technologies, LP Due to...
The Issue: GE Inspection Technologies, LP ("GE") has discovered that certain of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AccuLIF PL Tubing Set and AccuLIF TL Tubing Set AccuLIF Recalled by Stryker...
The Issue: There were two potential interference conditions identified with the way the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panorama Patient Monitoring Network. Software Kit 0020-00-0205-19A Recalled...
The Issue: An issue with the Panorama Central Station may cause the system to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Liberty Cycler-Peritoneal Dialysis Cycler Model: 180111 and...
The Issue: The door latch may not fully close and the door may open unexpectedly. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.