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 Apr 29, 2015
The PCA 3 infusion pump allows clinicians, or patients, to (self) Administer analgesia safely and effectively within…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 29, 2015
DBX Mix, 20 cc, Product Code: 058200. Demineralized Bone Matrix Mix, bone void filler.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Musculoskeletal Transplant Foundation, Inc.
FDA (openFDA device enforcement)
Reported Apr 29, 2015
Sony Medical Monitor LMD-1951MD 19 inch
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sony Latin America
FDA (openFDA device enforcement)
Reported Apr 29, 2015
Fluid Management System P4000; for irrigation and fluid warming in laparoscopic procedures, and distention, fluid…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thermedx LLC
FDA (openFDA device enforcement)
Reported Apr 22, 2015
Master Drug Library Software version 8.0, Product Code 35723V080, to be used with SIGMA Spectrum Infusion System (Pump)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
FDA (openFDA device enforcement)
Reported Apr 22, 2015
3i T3 Non-Platform Switched Tapered Implant Rx Only; 3.25 x 8.5 - 15.0 mm Dental Implants.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet 3i, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 22, 2015
LOW PROFILE NON-LOCK SCREW; 2.7mm x 22 mm; REF 131227222; LOT RM105E. Provides the orthopaedic surgeon a means of bone…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
FDA (openFDA device enforcement)
Reported Apr 22, 2015
WALLACH LL 100 cryosurgical units: LL100 Cryosurgical - Part Number 900001; LL110 with Pinned Yoke - Part Number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Apr 22, 2015
Culinary Masters, SCHWARMA SPICE BLEND 1/50 LB, Shelf Life: 180 days.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Gourmet Foods International
32 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 22, 2015
Kraft Macaroni & Cheese Boxed Dinner Original Flavor, 7.25oz.,packaged in blue and yellow cardboard box. There are four…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kraft Foods Group Inc.
FDA (openFDA food enforcement)
Reported Apr 22, 2015
PureLife Naturals Adult Multi-Plus Multi-Vitamins & Minerals Plus Herbs, 60 Pure Caps HDPE bottle
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ReNew Life Formulas, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 22, 2015
GROUND CUMIN, Net Wt. 5 lbs (2.3 Kg), UPC 7 52186 82560 0.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sahadi Fine Foods, Inc.
FDA (openFDA food enforcement)
Reported Apr 22, 2015
Talon Grasping Device, 160 cm, US endoscopy. Used for retrieval of foreign bodies, tissue specimens, stones or calculi…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.US Endoscopy Group Inc.
FDA (openFDA device enforcement)
Reported Apr 15, 2015
Instrument Kit for use with OsteoSponge SC grafts. The Instrument Kit is used to insert OsteoSponge SC grafts to fill…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bacterin International, Inc.
FDA (openFDA device enforcement)
Reported Apr 15, 2015
VasoNova Vascular Positioning System (VPS ) G4 Console Catalog number VPS-G4C Cardiovascular: The VPS Stylet and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.VasoNova, Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2015
ToggleLoc; fastener, fixation, non degradable, soft tissue; Artificial Ligament Fixation Device #7 PE Ziploop Extended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Bard 100% Latex-Free Urinary Drainage Bag with Anti-Reflux Chamber and Bard EX-Lok Sampling; Product Code 154006: Lot #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2015
French Broad Chocolates, Bubbie's Almond Bar, 60g (2.1 oz) bar, with aluminum foil with polyester ribbon & paper outer…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.French Broad Luscious Chocolates
FDA (openFDA food enforcement)
Reported Apr 8, 2015
GE Healthcare, Aespire 7900, Aespire View Anesthesia Machines. Model numbers 1009-9012-000. Intended to provide general…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Medtronic Dual Chamber Temporary External Pacemaker, Model 5392. Product Usage: The temporary pacemaker is used with a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc. Cardiac Rhythm Disease Management
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Hellas Golden Double Smoked Herring Vacuum Karagounis Bros SA -Hellas -35 A.3 - C.E. 2nd Industrial Zone -37500 VOLOS…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Moscahlades Bros Inc.
FDA (openFDA food enforcement)
Reported Apr 8, 2015
Vitagel; indicated in surgical procedures (other than in neurosurgical and ophthalmic) as an adjunct to hemostasis when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthovita, Inc., dba Stryker Orthobiologics.
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Autoject E1 Fixed needle device, Model Number AJ1310, UPC Code 384701310010 The Autoject E1 is an injector used by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Owen Mumford USA, Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2015
MR. HYDE INTENSE ENERGY PRE WORKOUT, Green Apple Natural and Artificial Flavor Dietary Supplement Net Weight 8.0 OZ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ProSupps USA LLC
FDA (openFDA food 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.