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.
4,689 stored notices name North Carolina, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach North Carolina too — those are in the archive.
Reported Sep 25, 2019
MiCal brand YELLOWFIN TUNA POKE CUBE, Raw, Frozen, Product of Vietnam, Wild Caught. Cube size - 1 inch (2cm x 2cm) AAA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stavis Seafoods, Inc.
FDA (openFDA food enforcement)
Reported Sep 25, 2019
Hemospray Endoscopic Hemostat
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wilson-Cook Medical Inc.
FDA (openFDA device enforcement)
Reported Sep 20, 2019
Astrochef LLC. Retira Platos Preparados De Pollo Estilo Pub Debido A Un Error De Rotulación Y Alérgenos No Declarados
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pegasus Foods Inc.
USDA FSIS
Reported Sep 18, 2019
Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Nutrition, Division
FDA (openFDA food enforcement)
Reported Sep 18, 2019
Natrelle, Saline-Filled Breast Implant Biocell Full Height with Fill Tube, Sterile, for the following style numbers:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Allergan PLC
14 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 18, 2019
YoCrunch VANILLA LOWFAT YOGURT WITH SNICKERS PIECES 4 - 4 oz (113g) - 16 oz (453g) 6 packaged or 4 cups per case. UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Danone Waters
FDA (openFDA food enforcement)
Reported Sep 18, 2019
Martha White Gluten Free Sweet Yellow Cornbread & Muffin Mix packaged in a 7oz. pouch. 12 pouches per wholesale case.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hometown Food Company
FDA (openFDA food enforcement)
Reported Sep 18, 2019
Plastic Bottles labeled with: "Ancient Youth Secret - Since 500 B.C., DR. NARAM'S RASAYANA D TABLET, Calcium Supplement…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Jivan Shakti Inc.
FDA (openFDA food enforcement)
Reported Sep 18, 2019
PediaSmart Organic Soy Vanilla Beverage Mix, 12.7 oz. (360g) composite can
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natures One Inc.
FDA (openFDA food enforcement)
Reported Sep 18, 2019
XP- CR Tibial Tray- Interlok 59mm Item # 195268
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
34 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 17, 2019
Perdue Foods LLC Retira Del Mercado Productos De Pollo Congelados Listos Para Consumir De Simply Smart Organics Debido…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Perdue Foods LLC
USDA FSIS
Reported Sep 11, 2019
Alere Cholestech LDX Analyzer, model # 14-874 containing power supplies with the identifying codes of 1837d and 1843d -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alere San Diego, Inc.
FDA (openFDA device enforcement)
Reported Sep 11, 2019
ES1725KFXN ESPOCAN SPINAL/EPID TRY NRFIT Catalog # 339114
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 11, 2019
Alaris EtCO2, Model 8300, UDI: 10885403830013, CareFusion for models 11634567 and 8300ADXeN933
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Sep 11, 2019
Norm-O-Temp model 111Z
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cincinnati Sub-Zero Products LLC, a Gentherm Company
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 11, 2019
Lipton DIET ICED TEA PEACH 6/16.9 oz plastic bottles MANUFACTURED BY INDEPENDENT PRODUCERS FOR THE PEPSI/LIPTON TEA…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Pepsi Bottling Ventures, LLC
FDA (openFDA food enforcement)
Reported Sep 11, 2019
Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel, a component of Berchtold Chromophare Ceiling Mounted…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Communications
FDA (openFDA device enforcement)
Reported Sep 4, 2019
EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product Code:5905190, 14.5 Fr. Alphacurve Catheter with Standard Kit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
27 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 4, 2019
All colors and sizes of Confectionery Arts International, LLC brand Jewel Dust, a pearlescent pigment, manufactured and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Confectionery Arts International, LLC
FDA (openFDA food enforcement)
Reported Sep 4, 2019
FLEXIBLE NEURO-FIBERSCOPE, 3.7MM X 34CM, Model # 11282BN1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Sep 4, 2019
Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is fully integrated and automated instrument including…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Phadia Ab
FDA (openFDA device enforcement)
Reported Sep 4, 2019
PreGel Lemon 50 4.4 lb (2kg) bag, Ingredients: dextrose, citric acid, mono and diglycerides of fatty acids, propane…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PreGel America, Inc.
FDA (openFDA food enforcement)
Reported Sep 4, 2019
Artis zee and Artis Q/ Q.zen Interventional Fluoroscopic X-Ray System with patient tables as follows: Systems Material…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 28, 2019
ZYMUTEST HIA MonoStrip, IgG ELISA kit, Model No. RK041A, for in vitro diagnostic use.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aniara Diagnostica LLC
1 more product in this recall
FDA (openFDA device 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.