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 8661–8680 of 29,737 recalls
Recalled Item: LineSider Spinal System 5.5/6.0mm Recalled by Integrity Implants Inc. Due to...
The Issue: Potential for weld separation of the Upper Tulip Head component from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panther Fusion Extraction Reagent-X Recalled by Hologic, Inc Due to Failed...
The Issue: Failed stability specifications for reagent kits that may result in false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains two...
The Issue: Excessive ultraviolet-C radiation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LineSider Spinal System 5.5/6.0mm Recalled by Integrity Implants Inc. Due to...
The Issue: Potential for weld separation of the Upper Tulip Head component from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD SURESTEP INTERMITTENT CATHETER TRAY Recalled by C.R. Bard Inc Due to...
The Issue: There is a potential to leak from the catheter where it connects to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD SURESTEP INTERMITTENT CATHETER TRAY Recalled by C.R. Bard Inc Due to...
The Issue: There is a potential to leak from the catheter where it connects to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E25Bio COVID-19 Direct Antigen Rapid Test Recalled by E25Bio, Inc. Due to...
The Issue: The Test is not authorized, cleared, or approved by FDA for clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: meridian bioscience immunocard STAT! Rotavirus test Recalled by MEDLINE...
The Issue: The product was incorrectly shipped at room temperature rather than .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntraSight Mobile IVUS Systems Recalled by Volcano Corp Due to...
The Issue: Multi-Modality Touch Screen Modules (MM-TSM), which are bedside/secondary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6" Recalled by...
The Issue: Guidewire included with two lots of Arterial Line Kits would not fit through...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Footrest ( use exclusively in combination with Intelli-C devices)...
The Issue: Friction rubber block in the clamping mechanism was missing in the Footrest....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Cranial Access Kits- indicated when a craniotomy is required Recalled...
The Issue: Incorrect extended expiration dates identified on the outer box label only,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuMoDx Flu A-B/RSV/SARS-CoV-2 Vantage Test Strip Recalled by NeuMoDx...
The Issue: A risk for product contamination was identified for the affected product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Cranial Access Kits- indicated when a craniotomy is required Recalled...
The Issue: Incorrect extended expiration dates identified on the outer box label only,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATRAUMATIC ADULT LUMBAR PUNCTURE TRAY Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BenchMark ULTRA and DISCOVERY ULTRA Instruments Recalled by Ventana Medical...
The Issue: Potential for Fluid Leak inside a staining system that could cause an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Sight OLO device is a computer vision based platform Recalled by SIGHT...
The Issue: In instances where custom ranges were configured on the device post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFE-T PLUS LUMBAR PUNCTURE TRAY ADULT Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray Recalled by Bard...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMBAR PUNCTURE TRAY ADULT 22G X3.5 STRL Recalled by Bard Peripheral...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.