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. 2,563 recalls have been distributed to Minnesota in the last 12 months.
Showing 17361–17380 of 29,186 recalls
Recalled Item: NOVAPLUS* Endotracheal WET PAK* Closed Suction System for Adults with...
The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...
The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WECK(R) from TELEFLEX Auto Endo5(R) Recalled by Teleflex Medical Due to The...
The Issue: The product has a non-conformity that may cause clips to mislead, jam or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T Recalled by Fresenius Medical Care Renal Therapies Group, LLC Due to...
The Issue: While reviewing documentation for the next software release of the 2008T, an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MONTERIS MEDICAL NEUROBLATE SYSTEM Recalled by Monteris Medical Corp Due to...
The Issue: The firm received complaints that involved an unanticipated interaction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Network Firewall (Cisco ASA 5506) Recalled by Philips Electronics...
The Issue: Firewall installed with Philips IntelliVue Information Center iX or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESONATE X4 CRT-D Recalled by Boston Scientific Corporation Due to The...
The Issue: The devices have an incorrect firmware configuration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOMENTUM X4 CRT-D Recalled by Boston Scientific Corporation Due to The...
The Issue: The devices have an incorrect firmware configuration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESONATE EL ICD DR Recalled by Boston Scientific Corporation Due to The...
The Issue: The devices have an incorrect firmware configuration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESONATE EL ICD VR Recalled by Boston Scientific Corporation Due to The...
The Issue: The devices have an incorrect firmware configuration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIGILANT X4 CRT-D Recalled by Boston Scientific Corporation Due to The...
The Issue: The devices have an incorrect firmware configuration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Shaft hip and anatomical shoulder instrument used for preparation...
The Issue: The Sirus Drill and Flexible Shaft instruments may not be adequately cleaned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sirus Drill 13mm diameter trauma instrument used for preparation of Recalled...
The Issue: The Sirus Drill and Flexible Shaft instruments may not be adequately cleaned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Difco" Agar Noble Recalled by Becton Dickinson & Co. Due to Mislabeling
The Issue: HighPuragar was mislabeled and inadvertently sold as Noble Agar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Go.Up computed tomography (CT) x-ray system table Recalled by...
The Issue: The table may become unstable if the nuts on the bolts were not adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemosphere System with the following three components: HEM1 Advanced Monitor...
The Issue: Pre-procedural issues related to software defects
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Go.Now computed tomography (CT) x-ray system table Recalled by...
The Issue: The table may become unstable if the nuts on the bolts were not adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm¿ O2 interventional fluoroscopic x-ray system Recalled by Medtronic...
The Issue: During servicing of certain internal components of the O-Arm O2 Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Complete Knee System Recalled by Zimmer Biomet, Inc. Due to Knee...
The Issue: Knee implant components (tibial bearings) are labeled with the incorrect size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.