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 Jan 22, 2020
Tobago Keys brand Coral Ridge Seafood Dipping Sauce 12 FL.OZ. (355 ml) and Peruvian Gold Grilling Sauce 12 FL.OZ (355…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Endorphin Farms, Inc.
FDA (openFDA food enforcement)
Reported Jan 22, 2020
Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for cementless and/or cemented fixation within the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported Jan 22, 2020
LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2020
Teleflex MEDICAL RuSCH One piece Male External Regular Catheter W/O Tape, REF A1500
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teleflex Medical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2020
Signature Crab Cake, Signature Crab Cake (2 pk), and Signature Crab Cake (4pk); Wegmans Ready to Cook Signature Crab…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wegmans Food Markets, Inc.
21 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 15, 2020
ImplantDirect InterActive Precision IO Scan Adapter, Part #6534-09PT, Platform: 3.4mm, Non-Sterile, Rx. The firm name…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 15, 2020
Medical convenience trays and kits, labeled as: Medical Action Industries, Inc.: ***CVC*** Clear Sequence Change Kit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Action Industries, Inc. 306
FDA (openFDA device enforcement)
Reported Jan 15, 2020
NANCY ADAMS DARK CHOCOLATE Graham Crackers, NET WT 7.5 OZ (212G); UPC 618645275860; packaged in a brown paper bag with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nassau Candy Distributors, Inc.
FDA (openFDA food enforcement)
Reported Jan 15, 2020
Cios Alpha, Model Number 10308191; mobile X-Ray system designed to provide X-ray imaging of the anatomical structures…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jan 15, 2020
GREY GHOST BAKERY scratch-made cookies LEMON SUGAR NET WT 1.4 OZ (40 G), UPC 8 53152 00308 1 , 4 OZ (113 G) UPC 8 53152…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TFI Holding dba Grey Ghost Bakery
FDA (openFDA food enforcement)
Reported Jan 8, 2020
i-STAT cTnI cartridge
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Point Of Care Inc.
FDA (openFDA device enforcement)
Reported Jan 8, 2020
Invia Foam Dressing Kit with FitPad - X-Large (3 pcs) SKU # 0876224. The Invia Foam Dressing Kit with FitPad consists…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medela Inc.
FDA (openFDA device enforcement)
Reported Jan 8, 2020
O-arm" O2 Imaging System, Product Number/CFN: BI-700-02000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.-Littleton
FDA (openFDA device enforcement)
Reported Jan 8, 2020
HeartMate 3 Mobile Power Unit, REF 107754, UDI or GTIN: 00813024010883, and 107758, UDI or GTIN: 00813024010890, when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec Corp.
FDA (openFDA device enforcement)
Reported Jan 1, 2020
STA UNICALIBRATOR (ref. 00675)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diagnostica Stago, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2020
Trader Joe's 8pcs Spicy California Roll, 8oz, SKU 00348966T
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fuji Food Products, Inc.
22 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 1, 2020
Babi.Plus 12.5 cm H2O Pressure Relief Manifold, REF 1030, RX Only, UDI: 04710810093562
High riskUsing this product could cause serious injury, illness or death — stop using it now.Galemed Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2020
ElectroTek Temporal Sensor Cable Gold - Long Length, Graduated - Product Usage: The electroencephalographic system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lifelines Neuro Company
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2020
Suantianyangmei Waxberry, 8.11 OZ (230g) clear plastic containers, UPC 6948576407226 and 3.12.2020 stamped on the box
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lin's Waha International Corp.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 1, 2020
VNS Therapy, SenTiva, Model # 1000, (01)05425025750405, Rx Only for vagal nerve stimulation (VNS) therapy
High riskUsing this product could cause serious injury, illness or death — stop using it now.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Jan 1, 2020
Snapshot Tracker Kit, Mas2659-01, KIT0898, Rx Only, Non Sterile, UDI: 07290109181868
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mazor Robotics Ltd.
FDA (openFDA device enforcement)
Reported Jan 1, 2020
PTS Panels CHOL+HDL+GLU Test Strips, Reference Number 5412, for use on CardioChek PA or CardioChek Plus analyzers
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Polymer Technology Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 1, 2020
RayStation stand-alone software treatment planning system, Model Numbers 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Dec 25, 2019
Natrelle Saline-Filled Breast Implant, for the following Styles and sizes, Style LP, Style 68 HP, Style 68 MP, Style…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Allergan PLC
3 more products 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.