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. 1,920 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,920 in last 12 months

Showing 2266122680 of 29,737 recalls

Medical DeviceAugust 27, 2015· Becton, Dickinson and Company, BD Biosciences

Recalled Item: CD4 (SK3) Recalled by Becton, Dickinson and Company, BD Biosciences Due to...

The Issue: CD4 FITC label contains an error in the Spanish small text - it states CD8 FITC.

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

Class III — Low RiskOngoing
Medical DeviceAugust 27, 2015· Zimmer, Inc.

Recalled Item: Zimmer Guide Wires for orthopedic procedures. Recalled by Zimmer, Inc. Due...

The Issue: Product labeling of these sterile guide wires (external carton label and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2015· Becton Dickinson & Co.

Recalled Item: BD AffirM VPIII Microbial Identification Test Recalled by Becton Dickinson &...

The Issue: BD has confirmed that a portion of tests associated with the affected lots(...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: syngo Lab Data Manager System - Product Usage: syngo Lab Recalled by Siemens...

The Issue: Software Issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2015· Edwards Lifesciences, LLC

Recalled Item: ThruPort Knot Pusher. This device is sold individually (Model KP1) Recalled...

The Issue: The configuration of the slot at the tip of the knot pusher may inhibit...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2015· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to...

The Issue: Cross-threading of the hemostasis valve may occur if it is tightened with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2015· Cardinal Health

Recalled Item: Ambitex NMD400 Nitrile Exam Gloves size medium. General Hospital and...

The Issue: Ambitex Nitrile NMD400 Exam Gloves size medium on exam hold were...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2015· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to...

The Issue: Cross-threading of the hemostasis valve may occur if it is tightened with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated Adult Pak P/N: 73124...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Teleflex Medical

Recalled Item: R¿sch Flexi-Slip Endotracheal Tube Stylet with Soft Distal Tip Recalled by...

The Issue: Due to reports of the plastic coating of the stylet splitting and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated Perfusion Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· C.R. Bard, Inc.

Recalled Item: Magic3 Intermittent Catheter with Sure Grip Hydrophilic Coated Silicone...

The Issue: Potential breach of the sterile barrier packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated PED/Adult Main Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated PED/Adult Main Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (750 tests) Part...

The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Teleflex Medical

Recalled Item: Rusch Flexi-slip tracheal tube Stylet Recalled by Teleflex Medical Due to...

The Issue: Due to reports of the plastic coating of the stylet splitting and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (100) tests Part...

The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (250) tests Part...

The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated Pediatric Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (400) tests Part...

The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...

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

Class II — Potential Health HazardOngoing