Product Recalls in North Carolina
Product recalls affecting North Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to North Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,064 recalls have been distributed to North Carolina in the last 12 months.
Showing 16641–16660 of 29,737 recalls
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: 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: 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: 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: 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: 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: Fortify 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: AMENDIA Omega Lumbar Interbody Fusion Device Recalled by Spinal Elements Due...
The Issue: Omega LIF interbody implants labeled as having 11 degrees of lordosis was...
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: 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: Unify 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: Advance¿ 35LP Low-Profile PTA Balloon Dilatation Catheter Recalled by Cook...
The Issue: Incorrect product labeling. Product labeled as 6mm x 2cm balloon are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter Recalled by...
The Issue: Device is at risk of having detectable levels of bacterial endotoxin present...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fortify 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: BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter Recalled by...
The Issue: Device is at risk of having detectable levels of bacterial endotoxin present...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.