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. 1,004 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,004 in last 12 months

Showing 30361–30380 of 54,363 recalls

Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Persona Stemmed Tibial Provisional Size H Right Recalled by Zimmer Biomet,...

The Issue: There is a potential for intermittent cracks in the raw material batch used...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Persona Cemented Tibial SZ PLT Size H Left Recalled by Zimmer Biomet, Inc....

The Issue: There is a potential for intermittent cracks in the raw material batch used...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Persona Stemmed Tibial Provisional Size H Left Recalled by Zimmer Biomet,...

The Issue: There is a potential for intermittent cracks in the raw material batch used...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Persona Cemented Tibial SZ PLT Size H Right Recalled by Zimmer Biomet, Inc....

The Issue: There is a potential for intermittent cracks in the raw material batch used...

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

Class II — Potential Health HazardOngoing
DrugAugust 4, 2017· Pfizer Inc.

Recalled Item: Quillivant XR methylphenidate HCl Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugAugust 4, 2017· Pfizer Inc.

Recalled Item: Quillivant XR methylphenidate HCl Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 4, 2017· Ultradent Products, Inc.

Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...

The Issue: The barcode label was placed underneath the sterile barrier and the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2017· ZOLL Medical Corporation

Recalled Item: OneStep CPR Complete Recalled by ZOLL Medical Corporation Due to A portion...

The Issue: A portion of one lot of ZOLL OneStep Complete Electrodes for adults will...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2017· Ultradent Products, Inc.

Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...

The Issue: The barcode label was placed underneath the sterile barrier and the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2017· Ultradent Products, Inc.

Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...

The Issue: The barcode label was placed underneath the sterile barrier and the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2017· Ultradent Products, Inc.

Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...

The Issue: The barcode label was placed underneath the sterile barrier and the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2017· Ultradent Products, Inc.

Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...

The Issue: The barcode label was placed underneath the sterile barrier and the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2017· OrthoPediatrics Corp

Recalled Item: Response 5.5/6.0 Spine System 7.0mm x 40mm Pedicle Screw Product Recalled by...

The Issue: The 7mm diameter uniaxial pedicle screws have been color anodized with the...

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

Class II — Potential Health HazardOngoing
DrugAugust 3, 2017· MEDLINE INDUSTRIES INC

Recalled Item: Vitamin A&D Ointment (petroleum 93.5%) Recalled by MEDLINE INDUSTRIES INC...

The Issue: Labeling Mixup; the individual A&D ointment foil packets are incorrectly...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 3, 2017· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Lorazepam Oral Concentrate Recalled by Amneal Pharmaceuticals of New York,...

The Issue: Defective Delivery System: the dropper measurement markings may be reversed,...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 3, 2017· KVK-Tech, Inc.

Recalled Item: Phentermine HCL Capsules Recalled by KVK-Tech, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: out-of-specification results...

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

Class III — Low RiskOngoing
Refund
DrugAugust 2, 2017· The Harvard Drug Group

Recalled Item: Rugby Diocto Liquid Recalled by The Harvard Drug Group Due to Microbial...

The Issue: Microbial contamination of Non-sterile Products; presence of yeast and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2017· The Harvard Drug Group

Recalled Item: Rugby Senexon Liquid Natural Vegetable Stimulant Recalled by The Harvard...

The Issue: Microbial contamination of Non-sterile Products; presence of yeast and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2017· The Harvard Drug Group

Recalled Item: Major Senna Syrup Natural Vegetable Laxative Recalled by The Harvard Drug...

The Issue: Microbial contamination of Non-sterile Products; presence of yeast and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2017· The Harvard Drug Group

Recalled Item: Rugby Aller-chlor (Chlorpheniramine Maleate Syrup Recalled by The Harvard...

The Issue: Microbial contamination of Non-sterile Products; presence of yeast and...

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

Class II — Potential Health HazardOngoing
Refund