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.
4,767 stored notices name North Carolina, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,868 notices were distributed nationwide, so they reach North Carolina too — those are in the archive.
Reported Sep 5, 2012
Tanimura & Antle Romaine Lettuce (Laitue Romaine) in plastic bag Wrapped Single Head Romaine marked Field Packed for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tanimura & Antle
FDA (openFDA food enforcement)
Reported Aug 29, 2012
UniCel DxH Slidemaker Stainer Instrument System, PN 775222. The DxH Slidemaker Stainer is a fully automated slide…
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 Aug 29, 2012
OPTETRAK LOGIC Proximal Tibial Spacer & Screws (2) 2.5 LT BLUE Size 2.5, 8mm***STERILE***Match insert/spacer/tray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2012
Processed Yellow Onions - Yellow Sliced 1/8", 1/4" and 3/16"
High riskUsing this product could cause serious injury, illness or death — stop using it now.Freshpoint Atlanta, Inc.
12 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 29, 2012
Hitachi Echelon MRI System/Oasis MRI, Software. These are software controlled MRI devices. Product Usage: The Echelon…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2012
Oysters, Frozen IQF, packaged in 5 lb bags, 6x5 lb/cartons, labeled in part ***Product of Korea***
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LD Amory & Company
FDA (openFDA food enforcement)
Reported Aug 29, 2012
Medtronic O-arm¿ Imaging System. Product Numbers: BI-700-00027-100, BI-700-00027-100R, BI-700-00027-120,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2012
syngo Dynamics Version 9.5
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions, USA, Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2012
Powered Mobility Offers Versatility (M¿V)TM Chair The Powered MOV Chair models EMS, EMS24, HHC, and INO Powered MOV…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 29, 2012
Serial interface module RS-232 Product Usage: The System 1 provides perfusion case data transfer through the use of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 22, 2012
DePuy Custom Implant Devices Packaging: Packaging was not standardized on customs, it was dependant on the geometry of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Aug 22, 2012
FunFresh Foods World Berry Organic Cacao Nibs 6 oz, packaged in blue, brown, red, white, black and green packaging with…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.FunFresh Foods Inc.
FDA (openFDA food enforcement)
Reported Aug 22, 2012
GE Healthcare Advantage Workstations, Advantage Worksation version 4.2 and 4.3 with Volume Viewer 2 (version 6.4-6.8)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Aug 22, 2012
Philips Essenta DR, X-Ray System, Diagnostic, general-purpose Model: 712070. The Essenta DR is a multifunctional…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Healthcare Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 22, 2012
Southern Home Pasta Salad Ranch with Bacon, 7.5 oz., UPC 0788002891, 12 packages per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Southern Home
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 22, 2012
Synthes(R) Hemostatic Bone Putty, Part numbers 08.901.001.97S, 08.901.001.98S, 08.901.001.99S, 08.901.001D, and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Synthes USA HQ, Inc.
FDA (openFDA device enforcement)
Reported Aug 22, 2012
TAUT, Cholangiogram Catheter Intraducer, Peritoneal Catheter, Teleflex Medical, Research Triangle Park, NC. An…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teleflex Medical
FDA (openFDA device enforcement)
Reported Aug 15, 2012
AngioDynamics Angiographic catheter --- Soft-Vu (JB-1) Non-braided. --- Size: 5F; Length: 100cm; designed to accept…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics Worldwide Headquarters
FDA (openFDA device enforcement)
Reported Aug 15, 2012
Tartar Sauce sold under the following brand names: 1) Golden Corral Tartar Sauce, 1 gallon,refrigerated Product Code:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ken's Foods, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 15, 2012
Philips MultiDiagnost Eleva with Flat Detector (MD Eleva FD)Model: 708034 Product Usage: Philips X-ray System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Healthcare Inc.
FDA (openFDA device enforcement)
Reported Aug 15, 2012
The ABL software version 6.12 for the ABL800 analyzer. The analyzers are intended for the in Vitro testing of: -Samples…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2012
Equinoxe Anatomic Replicator Plate Intended for Primary and Reverse Total Shoulder Arthroplasty
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2012
Integra¿ Advansys Medial Lisfranc Plate (MLP), Integra, 311 Enterprise Drive, Plainsboro, NJ 08536 The Advansys plates…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Aug 8, 2012
The Reliance 130 and 130L Cart Washer/Disinfector is a high capacity mechanical washer intended for use in the washing,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
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.