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. 997 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
997 in last 12 months

Showing 35741–35760 of 54,363 recalls

Medical DeviceJuly 1, 2016· Sysmex America Inc

Recalled Item: Fluorocell PLT reagent Recalled by Sysmex America Inc Due to There is a...

The Issue: There is a potential that fluorescent platelet (PLT-F) and immature platelet...

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

Class II — Potential Health HazardOngoing
FoodJuly 1, 2016· Coca-Cola Company (The)

Recalled Item: Huberts Lemonade Blackberry Recalled by Coca-Cola Company (The) Due to...

The Issue: The product may contain foreign material (glass) in some bottles.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2016· Coca-Cola Company (The)

Recalled Item: Huberts Lemonade Watermelon Recalled by Coca-Cola Company (The) Due to...

The Issue: The product may contain foreign material (glass) in some bottles.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2016· Coca-Cola Company (The)

Recalled Item: Huberts Original Lemonade Recalled by Coca-Cola Company (The) Due to Foreign...

The Issue: The product may contain foreign material (glass) in some bottles.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2016· Coca-Cola Company (The)

Recalled Item: Huberts Lemonade Strawberry Recalled by Coca-Cola Company (The) Due to...

The Issue: The product may contain foreign material (glass) in some bottles.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJune 30, 2016· Mister Cookie Face Corporation

Recalled Item: Sundae Shoppe Novelty Ice Cream Dipped "Variety"cones Recalled by Mister...

The Issue: Sundae Shoppe Novelty Ice Cream Dipped "Variety" Ice Cream Cones are being...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 30, 2016· Zimmer Biomet Spine, Inc

Recalled Item: Zyston¿ Transform Instrument Case. Model Number PCR8200-2101. Device labeled...

The Issue: Zimmer Bioment Spine, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2016· Zimmer Biomet Spine, Inc

Recalled Item: Zyston¿ Transform Implant Kit. Model Number PCR8200-3101. Device labeled...

The Issue: Zimmer Bioment Spine, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2016· Zimmer Gmbh

Recalled Item: Avenir M¿ller Stem 4 Standard Avenir M¿ller Stem 6 Lateral Recalled by...

The Issue: Product mix-up. The Avenir M¿ller Stem 6 lateral uncemented might be placed...

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

Class II — Potential Health HazardOngoing
DrugJune 30, 2016· Allergan Sales, LLC

Recalled Item: TAZORAC (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...

The Issue: Failed Content Uniformity Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 30, 2016· Actavis Inc

Recalled Item: Glipizide 2.5 mg Extended-release tablets Recalled by Actavis Inc Due to...

The Issue: Failed Dissolution Specifications: Glipizide 2.5 mg ER Tablets exceeded...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 30, 2016· Allergan Sales, LLC

Recalled Item: TAZORAC (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...

The Issue: Failed Content Uniformity Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2016· Isomeric Pharmacy Solution, LLC

Recalled Item: Methylprednisolone Acetate/Lidocaine HCl 40/10 mg/mL Injection Recalled by...

The Issue: Lack of Processing Controls: Isomeric Pharmacy Solution, LLC announces a...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 29, 2016· TYRX Inc.

Recalled Item: TRYX Neuro Absorbable Antibacterial Envelope Product Usage: Indicated for...

The Issue: TRYX products are being recalled since the processes of spaying, welding,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· TYRX Inc.

Recalled Item: TRYX Absorbable Antibacterial Envelope Product Usage: Indicated for...

The Issue: TRYX products are being recalled since the processes of spaying, welding,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· Winco Mfg., LLC

Recalled Item: TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming...

The Issue: Non-conforming component caused arms of TMM4 Stretcher chair to no longer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· Winco Mfg., LLC

Recalled Item: TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming...

The Issue: Non-conforming component caused arms of TMM4 Stretcher chair to no longer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· Winco Mfg., LLC

Recalled Item: TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming...

The Issue: Non-conforming component caused arms of TMM4 Stretcher chair to no longer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Recalled Item: ArjoHuntleigh Sara Combilizer Recalled by ARJOHUNTLEIGH POLSKA Sp. z.o.o....

The Issue: ArjoHuntleigh has concluded that a device tipping hazard may occur on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· C.R. Bard, Inc.

Recalled Item: SureStep Tray Recalled by C.R. Bard, Inc. Due to Labeling problem

The Issue: Labeling problem

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

Class III — Low RiskOngoing