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. 1,085 recalls have been distributed to North Carolina in the last 12 months.
Showing 14101–14120 of 29,737 recalls
Recalled Item: Replacement ECG leadwires with snap ends REF/Catalog Number Description...
The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex HUDSON RDI NEONATAL ConchaSmart Breathing Circuit with Dual Heated...
The Issue: Reported complaints of cracks being observed, prior to use, on swivel wye...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EliA RF IgM Well Recalled by Phadia Ab Due to Potential for reporting low...
The Issue: Potential for reporting low assay results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leadwire sets with snap ends: REF/Catalog Number Description 2106381-001 ECG...
The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replacement leadwires with grabber ends: REF/Catalog Number Description...
The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rim Plate Recalled by I.T.S. GmbH Due to The titanium implant has the wrong...
The Issue: The titanium implant has the wrong article number laser marked on it.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emerald Diluent Tubing Recalled by Abbott Laboratories Due to The diluent...
The Issue: The diluent tubing used on the instrument appears cloudy or to have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasal Alar SpO2 Sensor Recalled by Xhale Assurance, Inc. Due to These...
The Issue: These Instructions for Use has missing instructions related to the checking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RNeasy DSP FFPE Kit (48) Recalled by Qiagen Sciences, Inc. Due to The...
The Issue: The deparaffinization solution contains a contaminant, which leads to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Infusion Set Recalled by Becton Dickinson & Company Due to An...
The Issue: An incomplete occlusion can be caused by a variation in the wall thickness...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Samsung GM85 Mobile Digital X-ray Imaging System Product Usage: The Recalled...
The Issue: Potential issue related to the operation of the safety latch within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GETINGE MEERA MOBILE OPERATING TABLE: (1) Part 720001B2 (2) Part Recalled by...
The Issue: User may suffer an electric shock when coming in contact with the exposed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Connect Diabetes Management App Recalled by Roche Diabetes Care,...
The Issue: Users with Android OS 8.0 and above may be unable to transfer values...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Medical Technologies EndoTool IV Recalled by Monarch Medical...
The Issue: Insulin dosing calculations were erroneously high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OsteoSelect Demineralized Bone Matrix (DBM) Putty 10.0cc in a syringe...
The Issue: The firm received one customer complaint concerning three OsteoSelect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OAKWORKS Inc.Lithotripsy/Urology Table: CFLU401 Recalled by Oakworks Inc Due...
The Issue: Table assembly error with incorrect actuators for the lateral and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revive Reusable Bladder Support Recalled by Rinovum Women's Health Due to...
The Issue: The product is unable to meet the use life of 31 cycles and may split or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion MaxPlus Clear Needleless Connector. Intended for Positive...
The Issue: After disconnection of a luer, the valve of the connector remains recessed;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SenTec Membrane Changer (reloadable) [9 pcs] - Product Usage: Is Recalled by...
The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...
The Issue: There has been an increase in complaints related to leaks, suction issues,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.