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 Sep 7, 2016
Double Pump RF Patient Cassette; Product Number: 72204055. Intended to provide fluid distension and irrigation and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Vision Ab
FDA (openFDA device enforcement)
Reported Sep 7, 2016
Diamond Coated Tips and Burs are accessories to the Ultrasonic Scaler (VARIOS 350 LUX, VARIOS 350, VARIOS 150 LUX,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nakanishi Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 7, 2016
Allura Xper with release R8.2: Allura Xper FD10, 722026; Allura Xper FD10/10, 722027; Allura Xper FD20, 722028; Allura…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 7, 2016
Primo Fresh Serrano Peppers Distributed by Warren Produce, 824 W. Monte Cristo Rd, Edinburg, TX packaged in 1/4 bushel…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Warren Produce Co., LLC
FDA (openFDA food enforcement)
Reported Aug 31, 2016
BVX-330BR Bovie Precise 360 Handpiece 33cm, blade Product is used for the delivery of helium gas plasma for cutting,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bovie Medical Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.), 10' (3.05m) Cable, Catalog Number 51-7310.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Conmed Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Large QWIX Compression screw, dia. 7.5 mm L 90 mm, Lot No. FH86, Rx only, Product Usage: The QWIX Positioning screw is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Medtronic, Viva Quadripolar Implantable Cardioverter Defibrillators: Product Model VIVAXTCRT-D DTBA1D1, DTBA1D4…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Radiesse (+) Lidocaine, Injectable Implant 1.5cc, Rx only, P/N: 8063M0K1, Merz Aesthetics. Product Usage: RADIESSE is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merz North America, Inc.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Brilliance 64 CT Model number 728231 Product Usage: Computed Tomography X-ray systems intended to produce…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Conical portio adapter (acorn) small & large are used for examination and diagnosis in conjunction with endoscopic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Richard Wolf Medical Instruments Corp.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Infinite F50 instrument. The INFINITE F50 instrument is a 96-well absorbance reader for the measurement of light…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tecan US, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Ziehm Vision RFD 3D Mobile C-arm for Mobile Fluoroscopic Imaging
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ziehm Imaging Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 24, 2016
Xpert MRSA Catalog GXMRSA-120, Rev. AJ Microbiology: The Cepheid Xpert MRSA assay performed in the GeneXpert Dx System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cepheid
FDA (openFDA device enforcement)
Reported Aug 24, 2016
Haitai Matdongsan Peanuts Crunch Snack, Net Wt. 11.49 oz. (325gr), Imported and Distributed by: Haitai, Inc, 7227…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.H & E Trading Inc.
FDA (openFDA food enforcement)
Reported Aug 24, 2016
Summer Vegetable Salad with Seared Chicken, Garlic Croutons, and Mustard-Chive Vinaigrette
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hellofresh
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 24, 2016
Hospira RECEPTAL CANISTERS: 1L(1000mL), 1.5L(1500mL), 2L(2000mL) Canister, ATS, 2000, with Valve 1) List Numbers…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 24, 2016
OPTICAL BIOMETER AL-Scan: Software Version: 1.09 and earlier. Ophthalmic: The OPTICAL BIOMETER AL-Scan is a measuring…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nidek Inc.
FDA (openFDA device enforcement)
Reported Aug 24, 2016
OraQuick Ebola Rapid Antigen Test, Product Code 3001-2807; Intended for the qualitative detection of antigens for Ebola…
High riskUsing this product could cause serious injury, illness or death — stop using it now.OraSure Technologies, Inc.
FDA (openFDA device enforcement)
Reported Aug 24, 2016
IQF 1/4" Yellow Onion Dice, frozen, item numbers: 103364, 103381, and 104831, bulk cases, net wt. 45 lbs.; 11244CH…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oregon Potato Company
8 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 24, 2016
VITROS Immunodiagnostic Products TSH Reagent Pack, REF/Catalog Number/Product Code 191 2997, Unique Device Identifier…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Aug 17, 2016
NucliSENS easyMAG Magnetic Silica The NucliSENS easyMAG accessory products are reagents and disposable to be used with…
High riskUsing this product could cause serious injury, illness or death — stop using it now.BioMerieux SA
FDA (openFDA device enforcement)
Reported Aug 17, 2016
Medivance ArcticGel Neonatal Pad The pad is designed to fit into an incubator and provide whole body cooling for…
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 Aug 17, 2016
Hitachi Scenaria Computed Tomography System Hitachi Medical Systems America, Twinsburg, OH 44087
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America 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.