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. 1,098 recalls have been distributed to North Carolina in the last 12 months.
Showing 12001–12020 of 29,737 recalls
Recalled Item: Remisol Advance running Software Version 1.12 The Normand Info Remisol...
The Issue: Results from repeated run for WBC (White Bloodcell Count), UWBC (Urine Whit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover 100% Silicone Foley Catheter with Temperature Sensor 14FR 5CC2W...
The Issue: Temperature sensing catheters failed to meet the established calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover 400 ml 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley...
The Issue: Temperature sensing catheters failed to meet the established calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley Tray...
The Issue: Temperature sensing catheters failed to meet the established calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 640G Recalled by Medtronic Inc. Due to Missing solder battery...
The Issue: Missing solder battery connection, which could interrupt power of insulin pump.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Unity Recalled by Elekta, Inc. Due to potential risk that Legionella...
The Issue: potential risk that Legionella may be present in the Unity machine room,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 630G with SmartGuard Recalled by Medtronic Inc. Due to Missing...
The Issue: Missing solder battery connection, which could interrupt power of insulin pump.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover 400 ml 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley...
The Issue: Temperature sensing catheters failed to meet the established calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover 100% Silicone Foley Catheter with Temperature 16FR 5CC2W Recalled by...
The Issue: Temperature sensing catheters failed to meet the established calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover 400mL Recalled by Covidien Llc Due to Temperature sensing catheters...
The Issue: Temperature sensing catheters failed to meet the established calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Display Manager in the Artis Systems (Image-Intensified Fluoroscopic...
The Issue: Artis systems containing a Multi Display Manager of a specific lot, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe OmniBed with installed Servo Oxygen module. Infant incubator and...
The Issue: Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe Incubator with installed Servo Oxygen module. Infant incubator....
The Issue: Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillators Model numbers M3535A Recalled...
The Issue: HeartStart XL MonitorlDefibrillators may not have been included in prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DDU-2400EN Lifeline PRO Recalled by Defibtech, LLC Due to A component issue...
The Issue: A component issue may cause the AED to abort a shock delivery or reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DDU-2300 Lifeline/ReviveR View Recalled by Defibtech, LLC Due to A component...
The Issue: A component issue may cause the AED to abort a shock delivery or reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DDU-2450 Lifeline ECG Model Numbers DDU-A2450EN DDU-E2450DE DDU-E2450EN...
The Issue: A component issue may cause the AED to abort a shock delivery or reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1/4X3/16X3/16YCONN Recalled by LivaNova USA Inc. Due to The firm has...
The Issue: The firm has identified through internal tests that the sterile barrier of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3/8X3/8X3/8 Y CONN Recalled by LivaNova USA Inc. Due to XXX
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1/4X3/8 REDUC CONN Recalled by LivaNova USA Inc. Due to The firm has...
The Issue: The firm has identified through internal tests that the sterile barrier of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.