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 48,132 notices were distributed nationwide, so they reach Georgia too — those are in the archive.
Reported Feb 5, 2014
ZYM B Reagent (REF 70493) ZYM B reagent is an additional test used to reveal the results of some miniaturized…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux France Chemin De L'Or
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 5, 2014
Carestream DRX Evolution System (Standard Q) The DRX-Evolution System (Standard Q) is a permanently installed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carestream Health Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2014
KODAK DirectView DR 7500 Dual Detector System, MODEL DR 7500, Manufactured by Carestream Health, Inc. Made in U.S.A.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carestream Health, Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2014
The Centricity Laboratory System is intended to be an information system designed to support the clinical and…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.GE Healthcare It
FDA (openFDA device enforcement)
Reported Feb 5, 2014
Radial Assist RAD BOARD, used to support the weight of a patient's arm and supplies for a medical procedure. The Merit…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2014
Port Kit with Access Infusion Set under the following labels: 1) 8F/SL/Plastic Port/F, Product Number H965450140,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Navilyst Medical, Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2014
ARIATELE TELEMETRY TRANSMITTER, Model 96281, with SpO2 Option C. Model 96281 is intended for use with either adult or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, LLC
FDA (openFDA device enforcement)
Reported Feb 5, 2014
Teflon Tube, sterile T2 Humerus System Stryker Trauma GmbH Prof Kuntscher Str 1-5 24232 Sconkidrchen, Germany…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported Jan 29, 2014
DRX-Evolution with FF WS These products are permanently installed diagnostic x-ray systems composed of 4 main…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carestream Health, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 29, 2014
Civco Belly Board, Reusable non-sterile carbon fiber belly board with cushion, REF 125012, packaged 1 per box. Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Civco Medical Instruments Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 29, 2014
Composix L/P with Echo PS 10" X 13" Product Code 0144113 The Composix L/P Mesh with Echo PS Positioning System is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Davol, Inc., Subs. C. R. Bard, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 29, 2014
Heavenly Blue, (Raw milk, salt, culture, coagulant ), Flat Creek Lodge, 367 Bishop Chapel Church Rd, Swainsboro, GA…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Flat Creek Farm & Dairy
FDA (openFDA food enforcement)
Reported Jan 29, 2014
Puritan Bennett 840 Series Ventilator PB840 Operators Manual Addendum PN 066009A 09/02 The intended use of the oxygen…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nellcor Puritan Bennett Inc. (dba Covidien LP)
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 29, 2014
VITROS Chemistry Products COCM Reagent
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Jan 29, 2014
ADAC ARGUS Gamma Camera Systems & ADAC CIRRUS Gamma Camera Systems. Distributed by Philips Medical Systems, Cleveland,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 29, 2014
ABL90 FLEX Analyzer Radiometer Medical ApS, ¿kandevej 21 Br¿nsh¿j, Denmark A portable, automated analyzer that measures…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Jan 22, 2014
Locking Cortical Screw 3.5mmX38mm REF 8161-35-038
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
FDA (openFDA device enforcement)
Reported Jan 22, 2014
Centricity PACS System versions 3.X and higher and 4.X and higher Product Usage: The Centricity PACS Workstation is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ge Healthcare It
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2014
Hot Smoked Wine Maple Salmon, Item HS-B, vacuum packaged and either frozen or refrigerated, ranging in size between…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Josephson's Smokehouse
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 22, 2014
Leica BIOSYSTEMS; BOND Polymer Refine Red Detection; Catalog No: DS9390; Leica Biosystems Newcastle Ltd; Balliol…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Biosystems Newcastle Ltd.
FDA (openFDA device enforcement)
Reported Jan 22, 2014
pO2 D999 membrane units. Distributed by Radiometer America, Inc., Westlake, OH 44145 pO2 membrane units, ordering…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Jan 22, 2014
Palacos¿ R+G Radioplaque Bone Cement 1 x 40 g Single (with Gentamicin), 40.8 g Methyl Acrylate Copolymer, 20 ml Methyl…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Jan 15, 2014
Sandel Healthcare Safety Devices Weighted Safety Scalpel #3 Disposable Safety Handle with #10 Blade Manufactured for:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ansell Sandel Medical Industries LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 15, 2014
Arthrocare SPORTS MEDICINE, Knot Pusher, REF 25-3011, LOT #1049402, CON 1, 2013-10, NON-STERILE, Rx only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ArthroCare Medical 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.