All recall categories

Recalls distributed in North Carolina

These notices name North Carolina in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

4,767 stored notices name North Carolina, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,853 notices were distributed nationwide, so they reach North Carolina too — those are in the archive.

Medical devices

Reported Jul 29, 2015

Various OxyTOTE Portable Oxygen System regulators, Valve Integrated Pressure Regulator, one unit per package. Product…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Western / Scott Fetzer Company

FDA (openFDA device enforcement)

Medical devices

Reported Jul 22, 2015

Alere i flu, Alere i, Alere Influenza A & B; Part Number (PN) 425-024 The Alere" i Influenza A & B assay, performed on…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alere Scarborough, Inc. dba Binax, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 22, 2015

MOSAIQ Oncology Information System MOSAIQ is an oncology information system used to manage workflows for treatment…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 22, 2015

Allofix Insertion Kit, 2.0 mm, Single Drill, Product Usage: MTF Surgical Instruments are designed for the specific…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Musculoskeletal Transplant Foundation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 22, 2015

0210-312-000-Woundcare Replacement kit with soft tip; 0210-318-000; Woundcare Replacement with fan tip; 0210-318-100-…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Instruments Div.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 22, 2015

16mm Chisel Blade; used in the LCP Anterior Ankle Arthodesis Plate System and the Hip Preservation Surgery Set.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Synthes (USA) Products LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 22, 2015

Sysco International Whole Segments Mandarin Oranges In Light Syrup Net Wt. 6 LB 10 OZ (3.01 kg) NDC: 074865629065; 6…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Sysco Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Jul 22, 2015

ZNN Antegrade Femoral Nail (ZNN AF). Orthopedic internal fixation device.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 15, 2015

Bedessee Brown Betty BRAND COCONUT MILK Powder Mix, NET WT: 1) 1.76 OZ (50 g) and 2) 10.6 OZ. IMPORTED BY BEDESSEE…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Bedessee Imports, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 15, 2015

A.L.P.S. Foot Locking Calcaneus Plate,Small-Right. Provides the orthopaedic surgeon a means of bone fixation and helps…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biomet, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 15, 2015

Philips GoSafe Communicator 7000L Personal emergency response system.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Lifeline Systems, Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Jul 15, 2015

Breast Pack - contains Devon Light Glove Used during surgery

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stradis Healthcare, LLC.

50 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 15, 2015

DASANI Purified Water, 24/20 fl. oz. (1.25 pt) 591 mL, pack, Desani, The Coca Cola Company, Atlanta, GA 30313.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

World

FDA (openFDA food enforcement)

Medical devices

Reported Jul 8, 2015

Etest Cefotaxime CT 256 WW and Etest Cefotaxime CT 256 US. in vitro diagnostic.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioMerieux SA

FDA (openFDA device enforcement)

Food

Reported Jul 8, 2015

Ground Elk meat packaged individually for retail sale in hermetically sealed plastic with a black backing identified…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Frontiere Natural Meats

FDA (openFDA food enforcement)

Medical devices

Reported Jul 8, 2015

HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac transplantation in patient who are at risk of…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

HeartWare Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2015

Dr. Sheffield's LUBRI GEL 3 oz (85 g) Non sterile over-the-counter personal lubricant.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Sheffield Pharmaceuticals, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2015

Spine Wave Access Kit, Catalog Number 10-1530 Package contents: RLSP494-Rhythmlink Monopolar Stimulating Probe and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Spine Wave, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2015

Infinite F500, in vitro diagnostic. Product Usage: The Tecan Infinite F500 is a multifunctional microplate reader with…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tecan US, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2015

Natural Knee II Revision Femoral Stem, 125mm, item 6215-12-185. packaged in configuration 803/791. Knee Prosthesis…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2015

BLUE BELL COUNTRY COOKIE VANILLA ICE CREAM & CHOCOLATE CHIP COOKIE SANDWICH 5.75 FL OZ (170 mL)

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Blue Bell Creameries, LP

285 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 1, 2015

LapSac Surgical Tissue Pouch. The current intended use for the LapSac Surgical Tissue Pouch is for isolating tissue…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cook Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2015

SNOBIZ CHEESECAKE SHAVE ICE FLAVOR, 10 pouches/carton; 8 cartons/case (80 pouches total per case), 104 gram per pouch,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Crystal Fresh

FDA (openFDA food enforcement)

Food

Reported Jul 1, 2015

Deskins Candies, Chocolate No Bakes, Net Wt. 16-oz., packaged in 1 lb. plastic containers containing 8-10 cookies / 12…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Deskins Wholesale, LLC

FDA (openFDA food enforcement)

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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.