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. 1,824 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,824 in last 12 months

Showing 3978139800 of 54,363 recalls

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· STERILMED, INC.

Recalled Item: Zimmer Recalled by STERILMED, INC. Due to Mislabeling

The Issue: Sterilmed, Inc. is recalling its reprocessed Zimmer Tourniquet Cuff, Part...

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· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit Tubing Pack P/N: 66041-1 Terumo...

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 Perfusion Pack with...

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 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· 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 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· 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 (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· 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· 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
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· 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
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: HEPARIN Sodium in 0.45% Sodium Chloride Recalled by Cantrell Drug Company...

The Issue: Stability Data Does Not Support Expiry

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: fentaNYL CITRATE 4 MCG/mL in 0.9% SODIUM CHLORIDE Injection Recalled by...

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: fentaNYL citrate in 0.9% Sodium Chloride Injection Recalled by Cantrell Drug...

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: fentaNYL CITRATE 25 mcg/mL in 5% DEXTROSE Injection Recalled by Cantrell...

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: fentaNYL Citrate 50 mcg/mL in Sterile Water for Injection Recalled by...

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: fentaNYL citrate in 0.9% Sodium Chloride Injection Recalled by Cantrell Drug...

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund