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 Aug 31, 2022
Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2022
Nobel Biocare N1 TiUltra TCC NP 3.5x13mm
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nobel Biocare
FDA (openFDA device enforcement)
Reported Aug 31, 2022
NeuRx Diaphragm Pacing System (NeuRx DPS) External Pulse Generator (EPG), Part No. 23-0021.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Synapse Biomedical Inc.
FDA (openFDA device enforcement)
Reported Aug 24, 2022
Power electronic box, Part #AS-0066, subassembly for the MyoCycle MC-2.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Myolyn Inc.
FDA (openFDA device enforcement)
Reported Aug 24, 2022
Sweet Loren's Place and Bake Sugar Cookie Dough, Net Wt. 12 oz.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sweet Loren's
FDA (openFDA food enforcement)
Reported Aug 17, 2022
Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Implant Systems LLC
FDA (openFDA device enforcement)
Reported Aug 17, 2022
The Cholestech LDX¿ System combines enzymatic methodology and solidphase technology to measure total cholesterol, HDL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alere San Diego, Inc.
FDA (openFDA device enforcement)
Reported Aug 17, 2022
cobas e801 Immunoassay Analyzer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Aug 10, 2022
PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8360-10
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Implant Systems LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 10, 2022
The E-100 Generator (PN 374848-09) is a bipolar electrosurgical unit (ESU) designed to be used with the da Vinci Xi and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Aug 10, 2022
Dose Vital VIP Products Vital Honey With Caviar and Tongkat Ali Powder; 12 sachets-15g
High riskUsing this product could cause serious injury, illness or death — stop using it now.MKS Enterprise LLC
FDA (openFDA food enforcement)
Reported Aug 10, 2022
UroLift System REF UL400-4, QTY 4 Urolfit System with Handle Release Tool
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Neotract Inc.
FDA (openFDA device enforcement)
Reported Aug 10, 2022
Merlin PCS 3650 programmer Model 3330 software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St. Jude Medical, Cardiac Rhythm Management Division
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 10, 2022
Vicks Children's Botanicals Liquid Daytime/Nighttime Combo Pack 4oz plastic bottles
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Procter & Gamble Company
4 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 10, 2022
Turbett Surgical Container, TS1500
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Turbett Surgical, Inc.
FDA (openFDA device enforcement)
Reported Aug 3, 2022
REF: 4P52-20 Hemoglobin A1c for use with Architect, IVD, CE, R1 1 x 52 mL, R2 1 x 20 mL, A1cDL 2 x 35 mL
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 3, 2022
Da Vinci S/Si Large Clip Applier, Model 420230 Da Vinci S/Si Medium-Large Clip Applier, Model 420327 Da Vinci S/Si…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 3, 2022
Stryker 2.3mm Tapered Router, Catalog no. 5820-071-023 instrument used in craniotomy procedures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments
FDA (openFDA device enforcement)
Reported Aug 3, 2022
etouchus, model no. ETM-G01. Noninvasive Blood glucose meter.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Touch US LLC
FDA (openFDA device enforcement)
Reported Jul 27, 2022
ENDURO SPECIAL KEY TIB.LOCK.RING F1/10MM product code NP462R used with EnduRo Total Knee System. instrument used during…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Implant Systems LLC
13 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 27, 2022
Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress, REF P7924A01; and REF P7924ARENT01, PRO+ MRS Rental Surface with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 27, 2022
BD Connecta Stopcock with OFF Directed Tap Without Extension Tube (500 eaches/carton) Catalog No. 394910 (US)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
10 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 27, 2022
GreenLight HPSEA Laser Fibers, UPN 0010-2092
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Jul 27, 2022
LifeGlobal Fast Freeze Thawing Kit, Model No. GFT5-055
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
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.