Product Recalls in Wisconsin
Product recalls affecting Wisconsin — including food, drugs, consumer products, medical devices, and vehicles distributed to Wisconsin. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,624 recalls have been distributed to Wisconsin in the last 12 months.
Showing 16341–16360 of 28,744 recalls
Recalled Item: Alaris Infusion Pump administration sets labeled as: -Infusion Set Alaris...
The Issue: Complaints where users were unable to prime the administration set.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...
The Issue: Possible out of specification condition which may allow a bead component to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Go.Up Recalled by Siemens Medical Solutions USA, Inc Due to There is...
The Issue: There is a potential for a software issue that may cause the need for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Now Recalled by Siemens Medical Solutions USA, Inc Due to There...
The Issue: There is a potential for a software issue that may cause the need for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...
The Issue: Possible out of specification condition which may allow a bead component to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...
The Issue: Possible out of specification condition which may allow a bead component to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...
The Issue: Possible out of specification condition which may allow a bead component to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorin Stockert Heater-Cooler System 3T Recalled by LivaNova USA Due to Firm...
The Issue: Firm is notifying customers that the Deep-Cleaning Service is now available...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroAire SmartRelease Endoscopic System Recalled by MicroAire Surgical...
The Issue: The Instructions for Use (IFU) is incorrect with regards to sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Gentamicin Flex reagent cartridge Recalled by Siemens...
The Issue: The affected lots may exhibit inaccuracy for Quality Control and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VOLISTA StandOP (model 600) surgical lights shipped from October 2012...
The Issue: Potential keypad failure on VOLISTA StandOP Surgical Lights.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Gentamicin Flex reagent cartridge Recalled by Siemens Healthcare...
The Issue: The affected lots may exhibit inaccuracy for Quality Control and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRAD-3000E (Radrex-i) TFP-4336W (Wireless FPD) Recalled by Canon Medical...
The Issue: It was found when an operator performs a radiography using the wireless flat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BLAST Bandage Recalled by Tactical Medical Solutions, Inc. Due to Blast...
The Issue: Blast Bandages (part# BLAST) with Lot# 0617 were not terminally sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gyrus ACMI Reusable Active Cord for Bovie/ValleyLab Generators Recalled by...
The Issue: There is a potential for the cord to spark and cause a fire.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Promote Quadra Recalled by St Jude Medical Inc. Due to The firm is releasing...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ellipse Recalled by St Jude Medical Inc. Due to The firm is releasing new...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unify Assura Recalled by St Jude Medical Inc. Due to The firm is releasing...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: St. Jude Medical CONFIRM Rx Insertable Cardiac Monitor Recalled by St Jude...
The Issue: The firm is advising physicians that exposure to sub-freezing temperatures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unify Quadra Recalled by St Jude Medical Inc. Due to The firm is releasing...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.