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 Dec 24, 2014
Specialty Audible Torque Wrench Mfg by: Stryker Spine, Catalog number IS3002XLP, Non-sterile. Used to final tighten to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Spine
FDA (openFDA device enforcement)
Reported Dec 22, 2014
Recall Notification Report 086-2014 (Hickory Smoked Sliced Bacon)
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Recalling firm not stated
USDA FSIS
Reported Dec 17, 2014
Invacare Perfecto 2 V Oxygen Concentrator The finished device is packaged as a single unit. The service part contains a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Dec 17, 2014
Margaret Holmes Mixed Greens 14.5 oz, Distributed by McCall Farms, Effingham, SC
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mccall Farms Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 17, 2014
ESSENTIA Hydration Perfected Purified Water and Electrolytes, 9.5 pH, Manufactured for Essentia Water Inc., 22833…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nature's Way Purewater Systems, Inc.
FDA (openFDA food enforcement)
Reported Dec 17, 2014
Covidien Puritan Bennett 980 Ventilator, Rx ONLY, Made in Ireland., Covidien LLC, USA. REF 980X1ENDIUU.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nellcor Puritan Bennett Inc. (dba Covidien LP)
FDA (openFDA device enforcement)
Reported Dec 17, 2014
BrightView XCT is a gamma camera for Single Photon Emission Computed Tomography (SPECT) and integrates with an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Dec 17, 2014
Align Radial Stems, Prosthesis, Elbow, Hemi Replacement of the radial head for degenerative or post-traumatic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Skeletal Dynamics
FDA (openFDA device enforcement)
Reported Dec 17, 2014
Crocodile (size 3) are two-armed, wheeled walking aids, used by children with disabilities. Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Snug Seat Inc.
FDA (openFDA device enforcement)
Reported Dec 17, 2014
TomoTherapy Treatment System with software versions 2.0.1 / 2.0.2 / 2.0.3/ (Hi:Art 5.0.1 / 5.0.2 / 5.0.3)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TomoTherapy Incorporated
FDA (openFDA device enforcement)
Reported Dec 10, 2014
McGrath MAC2 Video Laryngoscope Blades Product supplied in box of 50 items, each individually peel-pouched and EtO…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aircraft Medical Limited
FDA (openFDA device enforcement)
Reported Dec 10, 2014
Amerigel Hydrogel Wound Dressing Wound management
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amerx Health Care Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 10, 2014
DASANI (R) PURIFIED WATER, 16.9 FL OZ (1.06 PT) 500 mL, BOTTLED BY A MEMBER OF THE COCA-COLA BOTTLERS' ASSOCIATION,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Coca Cola Bottling Company United, LLC
FDA (openFDA food enforcement)
Reported Dec 10, 2014
MAS CardioImmune XL Cardiac Marker Control; Model: CAI-XL1; intended for use in the clinical laboratory as an assayed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microgenics Corporation
FDA (openFDA device enforcement)
Reported Dec 10, 2014
Queso Seco Centroamericano (Cheese) in individually soft poly/plastic bags labeled in part: Lacteos Santa Martha Queso…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oasis Brands, Inc.
15 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 10, 2014
Gourmet Warehouse, Red Wine Marinade, 16 fl.oz. (473 mL), Ingredient: Soy Sauce, Salt, Black Pepper, Cayenne Pepper,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.R and S Gourmet Warehouse
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 10, 2014
Aquapak Adaptor, 028 NEB, INTL, Product No. 403128; Aquapak Adaptor, 033 NEB, INTL, Product No. 403133; Aqaupak…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 4, 2014
Nebraska Firm Recalls Pork Belly Product Produced Without Import Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nebraska Firm
USDA FSIS
Reported Dec 3, 2014
ARCHITECT Total T3 Reagent Kit (7K64) consists of: - 1 or 4 Bottle(s) (6.6 mL/27.0 mL) anti-T3 (sheep) coated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Ireland Diagnostics Division
FDA (openFDA device enforcement)
Reported Dec 3, 2014
Cannulaide, Model 101, 102, 103. Respirator. The Cannulaide product is composed of die-cut hydrocolloid-coated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beevers Manufacturing & Supply, Inc.
FDA (openFDA device enforcement)
Reported Dec 3, 2014
LUNA Chest, Model No. LU4006
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Novadaq Technologies, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 3, 2014
BrightView product code: 882478 BrightView X product code: 882480 BrightView XCT product code: 882482 and 882454
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 Dec 3, 2014
Trabecular Metal Tibial Impactor. Product Usage: TM Tibial Impactor pads are used in conjunction with the TM Tibial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 26, 2014
Etest¿ Ceftaroline (CPT32) WW B30. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Biomerieux
4 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.