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. 1,744 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,744 in last 12 months

Showing 4832148340 of 54,363 recalls

FoodOctober 8, 2013· Quaker Foods and Snacks North America

Recalled Item: White grits packaged in a paper bag labeled in part: Smooth & Creamy...

The Issue: Some Aunt Jemima brand Buttermilk Self-Rising Corn Meal Mix, Quick Grits...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 7, 2013· LAP of America Laser Applications, LLC

Recalled Item: CARINAsim MAN-1236 Rev 2 and CARINAiso MAN-1237 Rev 2 laser Recalled by LAP...

The Issue: Potential for patient to be marked incorrectly. Customers currently using...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2013· RTI Surgical, Inc.

Recalled Item: C-Plus" 10mm x 12mm Webless implants Pioneer Surgical's C-Plus " Recalled by...

The Issue: As the result of a recent internal review of regulatory documents, we have...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: User Defined Method Flex Assignment/Siemens Dimension Vista 500 or Dimension...

The Issue: When utilizing the Routine Inventory screen to enter a User Defined Method...

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

Class II — Potential Health HazardOngoing
DrugOctober 7, 2013· B @ B Trade Inc.

Recalled Item: Lidiy capsules Dietary Supplement. Each bottle contains 30 capsules....

The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 7, 2013· Amedra Pharmaceuticals LLC

Recalled Item: Dexedrine¿ (Dextroamphetamine Sulfate) Spansules¿ Sustained Release Capsules...

The Issue: Failed Dissolution Specifications: Out of Specification (OOS) test results...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 7, 2013· B @ B Trade Inc.

Recalled Item: Slim Fortune capsules Dietary Supplement. Each bottle contains 30 capsules....

The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 7, 2013· B @ B Trade Inc.

Recalled Item: Slim Expert softgel capsules Dietary Supplement. One month supply/ 30...

The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 7, 2013· Baxter Healthcare Corp.

Recalled Item: 1) The HomeChoice automated peritoneal dialysis system. Dataplate located on...

The Issue: In systems with version 10.4 software Initial Drain logic, the device will...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2013· Smith & Nephew Inc

Recalled Item: GENESIS(R) II Recalled by Smith & Nephew Inc Due to Swapped product....

The Issue: Swapped product. Non-porous tibial base size 5 L was mis-packaged as size 6...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2013· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Multi Parameter Patient Monitor (with Arrhythmia Detection and Alarms)...

The Issue: Mindray has identified an issue with V Series Monitor where the V Dock power...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2013· Smith & Nephew Inc

Recalled Item: GENESIS(R) II Recalled by Smith & Nephew Inc Due to Swapped product....

The Issue: Swapped product. Non-porous tibial base size 5 L was mis-packaged as size 6...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2013· Medtronic Vascular, Inc.

Recalled Item: Resolute Integrity Zotarolimus-eluting Coronary Stent: Stent ID 3.0 mm...

The Issue: A small number of units in lot number 0006573585 of the Resolute Integrity...

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

Class II — Potential Health HazardOngoing
FoodOctober 4, 2013· Ultra Laboratories

Recalled Item: Digestive Health Recalled by Ultra Laboratories Due to Ultra Laboratories is...

The Issue: Ultra Laboratories is recalling Digestive Health because a raw material used...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 4, 2013· Vitalab Co Inc

Recalled Item: VIT-RA-TOX Whole Beet Plant Juice Recalled by Vitalab Co Inc Due to Foreign...

The Issue: The firm reports a customer found a foreign object in the product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 4, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products COCM Reagent Recalled by Ortho-Clinical...

The Issue: Inaccurate quality control results.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2013· Biomet 3i, LLC

Recalled Item: ENDOBON XENOGRAFT GRANULES 0.5 ML (Bovine bone substitute) Endobon is...

The Issue: Individual pieces of a batch of Biomet's Endobon Xenograft Granules 0.5 ML...

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

Class III — Low RiskOngoing
Medical DeviceOctober 3, 2013· Advanced Sterilization Products

Recalled Item: STERITITE Containers: STERITITE Container Kit Recalled by Advanced...

The Issue: Advanced Sterilization Products (ASP) is recalling the SteriTite containers...

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

Class III — Low RiskOngoing
FoodOctober 3, 2013· Specialty Enzymes & Biotechnologies

Recalled Item: Cellulase: ACTA 4-702 APEX 17-6262 APEX 6-9762 ARTH EB 10831 Recalled by...

The Issue: Specialty Enzymes and Biotechnologies is recalling cellulase/mannanase and...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 3, 2013· Specialty Enzymes & Biotechnologies

Recalled Item: XYLANASE 150 Recalled by Specialty Enzymes & Biotechnologies Due to...

The Issue: Specialty Enzymes and Biotechnologies is recalling cellulase/mannanase and...

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

Class II — Potential Health HazardOngoing
Refund