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

54,363 total recalls
948 in last 12 months

Showing 42621–42640 of 54,363 recalls

FoodFebruary 6, 2015· MegaMex Foods, LLC - R&D Center

Recalled Item: Herdez Chilpotle Peppers Recalled by MegaMex Foods, LLC - R&D Center Due to...

The Issue: MegaMex Foods is recalling Herdez Chilpotle Peppers product due to an...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 6, 2015· Mars Food US

Recalled Item: UNCLE BEN'S(R) Ready Rice(R) NEW ORLEANS STYLE RED BEANS & RICE Recalled by...

The Issue: UNCLE BENS(R) Ready to Heat Pouches have the potential for containing metal...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 6, 2015· Mars Food US

Recalled Item: UNCLE BEN'S(R) Ready Rice(R) ROASTED CHICKEN FLAVORED with Carrots and Herbs...

The Issue: UNCLE BENS(R) Ready to Heat Pouches have the potential for containing metal...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 6, 2015· See's Candies Inc.

Recalled Item: See's Candies Classic Red Heart with Assorted Chocolates (8 oz. 227 g)...

The Issue: One packaging run of 8 oz. Classic Red Hearts with Assorted Chocolates was...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 5, 2015· Zipline Medical

Recalled Item: Zip 8i Surgical Skin Closure Device Recalled by Zipline Medical Due to The...

The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray systems Brilliance iCT Recalled by Philips Medical...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems Ingenuity Core 128. Intended to produce...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Arrow International Inc

Recalled Item: ARROW FiberOptix Intra-Aortic Balloon Catheter Kit Recalled by Arrow...

The Issue: Outer package product label incorrectly identifies the product as FiberOptix...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems Brilliance iCT SP. Intended to produce...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems Ingenuity CT scanners. Intended to produce...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Zipline Medical

Recalled Item: Zip 8M Wound Closure Device Recalled by Zipline Medical Due to The...

The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Zipline Medical

Recalled Item: Zip 16 Surgical Skin Closure Device Recalled by Zipline Medical Due to The...

The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems Brilliance CT 64-channel with Essence...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Derma Pen, LLC

Recalled Item: DermaPen Pro Model Recalled by Derma Pen, LLC Due to Derma Pen initiated a...

The Issue: Derma Pen initiated a field communication for Dermapen after receiving an...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems (Brilliance CT 64-channel w/Essence...

The Issue: Philips discovered that a software defect exists in marketed product wherein...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems Ingenuity Core. Intended to produce...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Synapse Cardiovascular I ProSolv CardioVascular Synapse...

The Issue: Under certain circumstances the patient Demographics in a report exported...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: FujiMedical Synapse Cardiovascular I ProSolv CardioVascular. A picture...

The Issue: Measurement values in the EMR may not accurately the actual measurement...

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

Class II — Potential Health HazardOngoing
FoodFebruary 4, 2015· Health One Pharmaceuticals Inc

Recalled Item: Reishi Mushroom Recalled by Health One Pharmaceuticals Inc Due to Health One...

The Issue: Health One Pharmaceuticals is recalling dietary supplements due to...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 4, 2015· Health One Pharmaceuticals Inc

Recalled Item: Polygala complex Recalled by Health One Pharmaceuticals Inc Due to Health...

The Issue: Health One Pharmaceuticals is recalling dietary supplements due to...

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

Class II — Potential Health HazardOngoing
Refund