Recalls distributed in Georgia
These notices name Georgia 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.
5,046 stored notices name Georgia, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Georgia too — those are in the archive.
Reported Mar 9, 2016
SENSE Body Coil 1.5T with identification; used in the ACS NT, Intera 1.5T and Achieva 1.5T MR system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
FDA (openFDA device enforcement)
Reported Mar 9, 2016
BrightView are gamma cameras; Designed for single or dual detector nuclear imaging.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 9, 2016
Gouda Cheese packaged under the brand names: Smith's Farmstead Gouda and Jansal Valley Mountain Gouda, Packaged in 11…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Smith's Country Cheese, Inc.
8 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 9, 2016
(Stryker) AccuPlace Straight Level Needle Guide; Assists the user with inserting a needle at a predetermined angle for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 5, 2016
Perdue Foods LLC, Retira Productos De Trozos De Pollo Empanado Por Posible Contaminacin Con Material Extrao
High riskUsing this product could cause serious injury, illness or death — stop using it now.Gold Creek Foods, LLC
USDA FSIS
Reported Mar 2, 2016
BD FMC7 FITC: Model 430918. FMC7 is intended for in vitro diagnostic use in the identification of cells expressing FMC7…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
Reported Mar 2, 2016
HipLOC CHS Plate/Lag Screw Introducer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
FDA (openFDA device enforcement)
Reported Mar 2, 2016
Convenience Kits from Centurion that contain an In-Vision- Plus Needleless IV Connector, Model: code RYM5001…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
FDA (openFDA device enforcement)
Reported Mar 2, 2016
Shuttle Select Slip-Cath Catheter. Angiographic catheter. For use in angiographic procedures as a conduit for the…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cook Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 2, 2016
Hill-Rom Bariatric Power Recliner, Product Model # P9096 Hill-Roms 660 lb Powered Bariatric Recliner was created to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
FDA (openFDA device enforcement)
Reported Mar 2, 2016
This reagent is for in vitro diagnostic use. Pax-5 (1EW) monoclonal antibody is intended to be used for the qualitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Mar 2, 2016
software for Syngo Dynamics a Picture Archiving and Communication System (PACS) intended for acceptance, transfer,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 24, 2016
REF 0038460 Toomey Syringe 70cc Syringe with Catheter Tip and Luer Tip Adapters, Single Use, Rx Only, Latex Free, 50…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Feb 24, 2016
Vitamin Supplement (Vial) D3, (cholecalciferol (vit D3)/lipoic acid/ubiquinol/…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Glades Drugs Inc.
FDA (openFDA drug enforcement)
Reported Feb 24, 2016
CEA / CD66e Ab-2, Product code RB-368-R7, RB-368-R1; 7 ml each. Description Carcinoembryonic antigen (CEA), is…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lab Vision Corporation
FDA (openFDA device enforcement)
Reported Feb 24, 2016
Covidien Endo GIA Ultra Universal 12 mm Short Stapler Handle Ref: EGIAUSHORT Product Usage: The Endo GIA Ultra…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 24, 2016
High Flow Irrigation Extender; Part Number 72201021. Arthroscopic accessories are indicated for use in access of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc., Endoscopy Div.
FDA (openFDA device enforcement)
Reported Feb 24, 2016
Eclipse Treatment Planning System versions 11, 13.0, 13.5 and 13.6; Model number: H48; Product Usage: The Eclipse…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Varian Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Feb 17, 2016
Endobon-Xenograft Granules, Zimmer Biomet, Synthetic Bone Grafting Material, used in dental and/or surgical procedures.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet France SARL
FDA (openFDA device enforcement)
Reported Feb 17, 2016
Arctic Sun 5000 and Arctic Sun 2000; Intended for monitoring and controlling patient temperatures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Feb 17, 2016
Whole cucumbers
High riskUsing this product could cause serious injury, illness or death — stop using it now.FreshPoint Corporate
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 17, 2016
Mavig Monitor Suspension System, Model GD60, contained in the following Fluoroscopic imaging systems: Advantx LCV+,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 17, 2016
Celestial Seasonings Roastaroma Herbal Tea Lot code: Best Before 20DEC17 Pack size: 6 retail units (20 count)/ per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hain Celestial Group
FDA (openFDA food enforcement)
Reported Feb 17, 2016
IMPLANT,TM, MTX 4.1 mm x 10 mm diameter 3.5 mm Catalog #TMM4B10 Product Usage: Zimmer Dental implant systems are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Dental Inc.
12 more products in this recall
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.