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.
4,748 stored notices name North Carolina, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach North Carolina too — those are in the archive.
Reported Oct 21, 2026Updated Oct 26, 2026
The ABL90 FLEX and ABL90 FLEX PLUS analyzers are intended for use by trained technologists, nurses, physicians and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
iFuse TORQ Implant System Model/Catalog Number: 10055T(10x55mm), 10060T(10x60mm), 10065T(10x65mm), 10080T(10x55mm),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SI-BONE, Inc.
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Mezzetta GOLDEN GREEK PEPERONCINI MEDIUM HEAT 32 FL OZ G.L. MEZZETTA, INC., AMERICAN CANYON, NAPA VALLEY, CA 94503…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.G L Mezzetta Inc.
FDA (openFDA food enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Product Name: Nihon Kohden CNS-6200 Series Central Nurse Station, Model/Catalog Number: CN-6201 Software Version:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nihon Kohden America LLC
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Onkos Surgical Inc. My3D Personalized Pelvic Implant, Porous, Left REF PV-ACREC-04M
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Onkos Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
28 oz. Gatorade Lemon Lime, Gatorade Lemon Lime Zero, Gatorade Orange, and Gatorade Orange Zero.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pepsico Inc.
FDA (openFDA food enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Spectral CT and Spectral CT 7500 RT; Software Version Numbers: 5.2.X (U.S.); 5.0.X, 5.2.X, 5.4.X (Outside U.S.); Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Battle Bandage, REF: 32-700; Patrol IFAK Bag, Black - Advanced, REF: 81-125-BL; Patrol IFAK Bag, Multicam - Advanced,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Safeguard US Operating LLC
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
McKesson CONSULT hCG Urine Cassette, Model/ Part: FHC-A102/5001; Alere hCG Cassette (20 mIU/mL) in Urine, Model/ Part:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alere San Diego, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 30" X 4" 2-LINE (CS 18) WHITE Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ASP Global, LLC.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
EnCor EnCompass Breast Biopsy and Tissue Removal System Console (model number: ENCPCONSOLE) and Driver (model number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
Systems/units containing affected software/SQL BECKMAN COULTER CHEMISTRY ANALYZER AU480 REF / UDI-DI code: B96692 /…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Mishima K.K.
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT, LAP CHOLE , Catalog Number: PGCGLCBAC; 2)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
VentStar Resus Neo. Neonatal. 25 Units per Box. Part Number: MP00310 Disposable breathing circuit for use with a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger, Inc.
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
HeartSine samaritan PAD (Public Access Defibrillator); HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.HeartSine Technologies Ltd.
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
NovaSeq 6000Dx including DRAGEN Server, Catalog Number: 20068232; Illumina DRAGEN Server for NextSeq 550Dx, Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Illumina, Inc.
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
Kofinas Garlic Mediterranean Infused Extra Virgin Olive Oil, packaged in 3.4 fl oz (100mL), 8.5 fl oz (250mL), and 17…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lmsi, LLC
FDA (openFDA food enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
Brand Name: Penumbra System (RED 62 Reperfusion Catheter) Product Name: Penumbra System (RED 62 Reperfusion Catheter)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Penumbra Inc.
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
In-Line Valve, Product Number: P5-TEE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Percussionaire Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
Salata Salad Kitchen Jalapen¿o Avocado Dressing. Keep Refrigerated. Packaged in the following sizes: 1. 12.5 fl. oz.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Salata Dressings, LLC
FDA (openFDA food enforcement)
Reported Oct 7, 2026
Cornea
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Saving Sight
FDA (weekly enforcement report)
Reported Oct 7, 2026Updated Oct 13, 2026
Computed Tomography X-ray System, Model: uCT 530 with software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shanghai United Imaging Healthcare Co., Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
Brand Name: Quantum PureFlow Product Name: Quantum PureFlow Standard Heat Exchanger High Flow 3/8 W Model/Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectrum Medical Srl
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.