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. 2,789 recalls have been distributed to North Carolina in the last 12 months.
Showing 8101–8120 of 29,737 recalls
Recalled Item: Trevo Trak 21 Microcatheter Recalled by Stryker Neurovascular Due to...
The Issue: Microcatheter product label on the carton is missing the microcatheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Service manuals for the CT Recalled by GE Healthcare, LLC Due to As a result...
The Issue: As a result of unclear guidance in the service manual, the table can drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YelloPort Elite Universal Seal. For use in laparoscopic procedures. Recalled...
The Issue: There is the potential that YelloPort Elite Universal Seals packaging may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivo 45LS Ventilator- intended to provide continuous or intermittent...
The Issue: A forced shutdown of one of the processors did not generate a watch dog...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker INFINITY Resect Guide for INBONE Talus Recalled by Wright Medical...
The Issue: The instrument is incorrectly color coded.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DVR Anatomic Recalled by CHANGZHOU BIOMET MEDICAL DEVICES CO., LTD. Due to...
The Issue: One lot of DVRASL plates were incorrectly etched and may have been placed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: GCX Channel Mounting Accessory Model/Catalog Number:...
The Issue: Under certain circumstances, the mounting screws may loosen or pull out from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Aisys CS2 Anesthesia System Recalled by GE Healthcare, LLC Due...
The Issue: There is a potential reversal of the O2 and air cylinder pressure transducer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 9B SP1. For radiation treatment planning. Recalled by RAYSEARCH...
The Issue: An issue with propagation of treatment course information from RayStation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventana HE 600 System Recalled by Ventana Medical Systems Inc Due to There...
The Issue: There is a potential for fluid leak inside the Ventana HE 600 instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Laser System Recalled by Spectranetics Corporation Due to The...
The Issue: The LAS-100 Laser system may detect an inoperable hardware component during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peak Universal Bond Self-Etch Bottle Kit Recalled by Ultradent Products,...
The Issue: SE primer may be missing some or all of the resin portion of the chemistry....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaturaLyte 2301 2K 3.0 Ca 1 Mg Gal Recalled by Fresenius Medical Care...
The Issue: The product was potentially exposed to below-recommended storage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xhibit Telemetry Receiver Recalled by Spacelabs Healthcare, Inc. Due to...
The Issue: Software related alarm escalation defect occurs after approximately 25 days...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuRx Diaphragm Pacing System (NeuRx DPS) Recalled by Synapse Biomedical Inc...
The Issue: Firm has revised labeling to consistently call out storage conditions and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GreenLight HPSEA Laser Fibers Recalled by Boston Scientific Corporation Due...
The Issue: Several complaints were received for the affected lot; users received a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaviCare Nurse Call/Voalte Nurse Call Recalled by Baxter Healthcare...
The Issue: An issue has been identified with Phillips (Emergin) and Longleaf non relay...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSSUR VARIFLEX SUBA JUNIOR foot and ankle external prosthesis Recalled by...
The Issue: Due to receiving complaints related to broken (cracked) prosthetic foot with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Avance CS2 Recalled by GE Healthcare, LLC Due to The base of...
The Issue: The base of the anesthesia system can have a crack and could potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HammerTube Implant Recalled by Paragon 28, Inc. Due to Due to Titanium...
The Issue: Due to Titanium plasma coating not present implant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.