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 26301–26320 of 29,186 recalls
Recalled Item: Steinmann Pin Recalled by MicroAire Surgical Instruments, LLC Due to A...
The Issue: A medical device used in surgical procedures was packaged in a pouch in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vygon 14 Microbore Extension Set with Bionector Recalled by Churchill...
The Issue: Microbore tubing disconnecting from male luers on the extension sets.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Dressing Change Kit Recalled by Churchill Medical Systems, Inc. Due...
The Issue: Microbore tubing disconnecting from male luers on the extension sets.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clinical Chemistry Phosphorus Reagent The Phosphorus assay is used for...
The Issue: Reagent lots 64736UN12, 03991UN13, 51611UN13, 74805UN12, and 03992UN13 have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T8 REMOVAL HEAD Recalled by Medtronic Sofamor Danek USA Inc Due to One lot...
The Issue: One lot of the T8 Removal Head had incorrect hardness specification, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis ADROIT 6F Guiding Catheter Product Usage: For intravascular...
The Issue: Due to a labeling error related to the conversion of the inner diameter of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model BP7507 OPTI LION E-Plus Cassettes 25 Cassettes with Sample Probes...
The Issue: OPTI LION E-Plus Cassettes were labeled with an incorrect barcode. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonogage EyeScan Recalled by Sonogage Inc Due to During an FDA inspection on...
The Issue: During an FDA inspection on 7/15-26/2013, it was discovered that the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VARISOURCE Breast Template System for high-dose rate Brachytherapy....
The Issue: The recall was initiated after Varian Medical became aware the Lexan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Easy Upgrade DR Recalled by Philips Healthcare Inc. Due to The...
The Issue: The mirror icon on the bottom of each image could be misinterpreted as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon 24 Large Titanium Clips with Adhesive Backing Recalled by Teleflex...
The Issue: The manufacturing and expiration dates are not printed on the blister pack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E-Z Clean¿ Disposable Laparoscopic Electrode Model Number 0100L and 0100LS....
The Issue: Megadyne Medical Products is recalling certain lots of E-Z Clean, L-Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enhancement Medical expression. model # EXP-150. Injectable Gel 1.5cc...
The Issue: Manufacturer made a change in the production process that resulted in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips MR Systems: Asset 0.5T Recalled by Philips Medical Systems...
The Issue: There is a potential for water to collect in the vent pipe elbow in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Ultrasound ViewPoint 6. Product Usage: ViewPoint is intended to Recalled...
The Issue: GE has recently become aware of a potential safety issue due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX Ultra HA 5.5 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX Ultra HA 4.5 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEORAPTOR 2.3 mm Suture Anchor with ULTRABRAID COBRAID Suture Recalled by...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX" Ultra 4.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX Ultra 6.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.