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.

54,363 total recalls
1,085 in last 12 months

Showing 13981–14000 of 29,737 recalls

Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER Recalled by Bard Peripheral...

The Issue: The action is being initiated due to complaints received concerning the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter Recalled by Bard Peripheral...

The Issue: The action is being initiated due to complaints received concerning the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded Stylet Recalled...

The Issue: The action is being initiated due to complaints received concerning the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER Recalled by Bard Peripheral...

The Issue: The action is being initiated due to complaints received concerning the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter Recalled by Bard Peripheral...

The Issue: The action is being initiated due to complaints received concerning the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter Recalled by Bard Peripheral...

The Issue: The action is being initiated due to complaints received concerning the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: EQUISTREAM XK Alphacurve Long-Term Hemodialysis Catheter REF/Product...

The Issue: The action is being initiated due to complaints received concerning the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Becton Dickinson & Company

Recalled Item: BD Vacutainer Fluoride Tubes for Blood Alcohol determinations Part Number:...

The Issue: Lot has been confirmed to have no additive within the tube. Sample processed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Medline Industries, Inc.

Recalled Item: Anti-fog solution packaged in a Tyvek peel pouch and it Recalled by Medline...

The Issue: The Anti-Fog Solution may not defog properly due to a degradation in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Galemed Corporation

Recalled Item: Babi.Plus 12.5 cm H2O Pressure Relief Manifold Recalled by Galemed...

The Issue: Reports of pressure relief manifold venting gas below the standard pressure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 30, 2019· Boston Scientific Neuromodulation Corporation

Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...

The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Boston Scientific Neuromodulation Corporation

Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...

The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Boston Scientific Neuromodulation Corporation

Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...

The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Boston Scientific Neuromodulation Corporation

Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...

The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing