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. 1,924 recalls have been distributed to North Carolina in the last 12 months.
Showing 21281–21300 of 29,737 recalls
Recalled Item: Merge Cardio software. Merge Cardio is a system intended to Recalled by...
The Issue: If images are sent without an order in the system, they will be matched with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Hemo software. Merge Hemo monitors Recalled by Merge Healthcare, Inc....
The Issue: There is a potential connection issue when powering up the Merge Hemo Record...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS software. Product Usage: Merge PACS (Picture Archiving...
The Issue: The software did not show unviewed images when the last view was skipped....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PneumoSure XL High Flow Insufflator and PneumoSure High Flow Insufflator...
The Issue: When operating the device in high flow mode (40L/min, 15 mmHg) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ DIAGNOSTIC ULTRASOUND SYSTEM Recalled by Philips Ultrasound, Inc. Due...
The Issue: The fasteners securing the control panel assembly to the base of the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific is voluntarily implementing a Medical Device Recall of one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB Sciex Triple Quad 4500MD LC/MS/MS System Recalled by Ab Sciex Due to...
The Issue: Under certain conditions, mass spectrometers may report incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuroBlate System SideFire Select 2.2 mm Directional Laser Probe Recalled by...
The Issue: Monteris received a report that the sapphire lens on a 2.2SF probe fractured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan Robotic Catheter Accessory Kits Recalled by Hansen Medical Inc Due...
The Issue: Firm's quarterly dose audit testing showed that one batch was radiated below...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein Single Use Syringe Luer-Lock Recalled by Becton Dickinson &...
The Issue: BD 10 mL Syringe Luer-Lok Tip with BD PrecisionGlide Needle 21G x 1 (0.8 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein Single Use Syringe Luer-Lock Recalled by Becton Dickinson &...
The Issue: BD 10 mL Syringe Luer-Lok Tip with BD PrecisionGlide Needle 21G x 1 (0.8 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoWrist Stapler 45 and Stapler 30 instruments used on the Recalled by...
The Issue: Potential for unexpected motion of the Xi Stapler jaws on the da Vinci Xi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance BigBore Radiology Computed Tomography X-ray systems Recalled by...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 Computed Tomography X-ray systems is intended to Recalled...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ARCHITECT Estradiol Kit Intended to measure estradiol Recalled by Abbott...
The Issue: Interaction of Fulvestrant with the ARCHITECT Estradiol assay, leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 16 Computed Tomography X-ray systems is intended to produce...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit Recalled by CareFusion 303, Inc. Due to The Alaris PC units...
The Issue: The Alaris PC units model 8015 may display a system error code 133.6080 due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance BigBore Oncology Computed Tomography X-ray systems Recalled by...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck EFx Classic Fascial Closure System Recalled by Teleflex Medical Due to...
The Issue: Incorrect expiration date was printed on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 Computed Tomography X-ray systems is intended to produce...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.