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 Jun 8, 2022
XVIVO Organ Chamber REF 19020
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Xvivo Perfusion Ab
FDA (openFDA device enforcement)
Reported Jun 1, 2022
SUR-FIT Natura S4S Durahesive Wafer 70MM (1X10PK) US. Each market unit contains 10 individual wafers.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConvaTec, Inc.
FDA (openFDA device enforcement)
Reported Jun 1, 2022
Invacare TDX SP2, Model Nos. TDXSP2 TDXSP2-MCG TDXSP2V
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Jun 1, 2022
ABX Pentra Calcium AS CP, Reagent 90 mL, REF A11A01954
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
FDA (openFDA device enforcement)
Reported Jun 1, 2022
Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with AdaptiveStim Technology Neurostimulator with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 1, 2022
Mrs. Miller's Homemade Jam Smokey BBQ Bacon Jam packaged into 9 oz glass jar 12 jars per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mrs Millers Homemade Jams LLC.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 1, 2022
INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew Orthopaedics GmbH
FDA (openFDA device enforcement)
Reported Jun 1, 2022
Surgical Suture Kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stradis Healthcare
FDA (openFDA device enforcement)
Reported Jun 1, 2022
(1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile; (2) Gibeck Humid-Vent 2S Flex DC, Product #17732,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 1, 2022
AC-powered adjustable medical beds with built-in electric DC actuators and controls.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Umano Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 25, 2022
Dragonfly OpStar Imaging Catheter, REF 1014651/1014652, 0.068 in, 0.014 in, 135 cm, STERILE EO
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abbott Vascular
FDA (openFDA device enforcement)
Reported May 25, 2022
NaviCare Nurse Call System provides a comprehensive communication and information system that places patient calls,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 25, 2022
MicroScan WalkAway-40 plus Instrument REF B1018-283
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 25, 2022
DOUX SOUTH PICKLES EAT WITH A SOUTHERN ACCENT BAKKAVOR CURRY CAULIFLOWER 5 GALLON
High riskUsing this product could cause serious injury, illness or death — stop using it now.Doux South Specialties LLC
FDA (openFDA food enforcement)
Reported May 25, 2022
Driscoll's Blackberries (Fresh) 12x6 oz, 12x12 oz, 12x10 oz, 2x8x18 oz Clamshell Distributed by Strawberry Associated,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Driscoll's Inc.
FDA (openFDA food enforcement)
Reported May 25, 2022
Getinge 9100-Series Washer Disinfector models: 9120E, 9125E, 9127E, 9128E, 9122EW, 9128EW.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge USA Sales Inc.
FDA (openFDA device enforcement)
Reported May 25, 2022
Gorton s Fish Sandwich Fillets, 18.3 OZ, UPC 44400 15440
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gorton's, Inc.
FDA (openFDA food enforcement)
Reported May 25, 2022
ATLAS Stim Headbox-NK For use only with the ATLAS Neurophysiology System. CAUTION--INVESTIGATIONAL DEVICE Limited by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Neuralynx Inc.
FDA (openFDA device enforcement)
Reported May 25, 2022
Radiometer, REF:956-552, PIC050- Arterial Blood Sampler 1 X 2 mL, 80 IU electrolyte-balanced heparin. Not for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported May 25, 2022
LEGION NARROW PS OXIN SZ 6N RT and JRNY II BCS FEMORAL OXIN LT SZ 5
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew Inc.
FDA (openFDA device enforcement)
Reported May 25, 2022
Total Resources International First Aid Kits, Item Numbers: 10HBC01087, 10HBC01092A3PK, 10HBC01112, 10HBC01113,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Total Resources Intl
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 18, 2022
VITEK 2 Systems and VITEK 2 with MYLA.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
FDA (openFDA device enforcement)
Reported May 18, 2022
putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe REF 700-010, PUTTY
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cerapedics, Inc.
FDA (openFDA device enforcement)
Reported May 18, 2022
The following first aid kits and cabinets containing components Medi-First XS Non-Aspirin, Product #80450, 2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Certified Safety Mfg Inc.
FDA (openFDA device enforcement)
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Other states
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.