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 Jan 21, 2015
Femto LDV Z-Generation Femtosecond Surgical Lasers are used to perform ophthalmic surgeries.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ziemer USA Inc.
FDA (openFDA device enforcement)
Reported Jan 16, 2015
Firma De Georgia Retira Productos De Carne Y Pollo Por Mal Etiquetado Y Con Alrgenos No Declarados
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kabobs Aquisition, LLC
USDA FSIS
Reported Jan 16, 2015
Georgia Firm Recalls Pork Products Due To Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Heywoods Group Corp.
USDA FSIS
Reported Jan 14, 2015
Abdallah Milk Chocolate Bites CARAMEL, Net Wt 4.5 oz. (127g), UPC 7 6668407116 2, Ingredients: Pure milk chocolate…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abdallah Candies, Inc.
FDA (openFDA food enforcement)
Reported Jan 14, 2015
Baxter Amia Automated PD systems are used in the treatment of adult renal failure patients to perform automated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 14, 2015
Chest Tube Tray (Cardiovascular Surgical Instruments convenience kit)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 14, 2015
CSA Medical truFreeze System; Model: CC3-01, a cryogenic surgical device ***The involved units are those with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CSA Medical
FDA (openFDA device enforcement)
Reported Jan 14, 2015
Cable remote control JUPITER U, Material no.4500119, Serial number: to (incl.) 102306915. Patient positioning during…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trumpf Medical Systems, Inc.
11 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 14, 2015
Vintage Pure Bee Flower Honey, Net Weight 16.4 oz (465g), Packaged in a Glass Jar, Product of Turkey, Imported by:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Vintage Food Corp.
FDA (openFDA food enforcement)
Reported Jan 7, 2015
Organic Cilantro Medium Bulk - size is dependent on customer request; Certified Organic by QAI High Quality Organics…
High riskUsing this product could cause serious injury, illness or death — stop using it now.High Quality Organics, Inc.
FDA (openFDA food enforcement)
Reported Jan 7, 2015
Hypodermic Needle Pro¿ Edge" Safety Device 20G x1; Reorder Number: 402010 Product Usage: The Needle Pro¿ Edge Safety…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 7, 2015
Pride of the Redlands brand Florida green skin avocado, 12ct,14ct, 16ct, 18ct, and 20ct packaged in 1/2 bushel boxes
High riskUsing this product could cause serious injury, illness or death — stop using it now.Unity Groves Corporation
FDA (openFDA food enforcement)
Reported Dec 31, 2014
Bausch & Lomb Stellaris PC w/ Laser, BL14304 The responsible firm name is Bausch & Lomb Incorporated Rochester, NY
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 31, 2014
KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 7.0 mm, Distributed by Kimberly Clark Global Sales, LLC.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Halyard Health
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 31, 2014
ADULT Radiotransparent Electrode, Part number C100-PHILIPS, Rx ONLY, For use with Philips HeartStart AED "Comparable to…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heart Sync, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 31, 2014
Illumina MiSeqDx Universal Kit 1.0, PN 15039608 The Illumina MiSeqDx Universal Kit 1.0 is a set of reagents and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Illumina Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 31, 2014
HemosIL PT-Fibrinogen HS PLUS, IVD --- Instrumentation Laboratory IL Company. A high sensitivity thromboplastin reagent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Laboratory Co.
FDA (openFDA device enforcement)
Reported Dec 31, 2014
DPM 6 Patient Monitor and DPM 7 Patient Monitor. The product affected is the Mindray IBP module, P/N is 6800-30-50485…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. dba Mindray North America
FDA (openFDA device enforcement)
Reported Dec 31, 2014
North Carolina Firm Recalls Canned Soup Products Due to Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.North Carolina Firm
USDA FSIS
Reported Dec 31, 2014
HemoCue¿ Glucose 201 Microcuvettes, The HemoCue Glucose 201 Microcuvettes are designed for use with the HemoCue Glucose…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Dec 24, 2014
Glucose Hexokinase (Liquid) Reagent For the in vitro quantitative determination of Glucose in serum.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.JAS Diagnostics Inc.
FDA (openFDA device enforcement)
Reported Dec 24, 2014
KOZY SHACK SIMPLY WELL CHOCOLATE, NET WT 4 OZ. Product packed in brown carton box, 48 individual units x 4 OZ. Keep…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kozy Shack Inc.
FDA (openFDA food enforcement)
Reported Dec 24, 2014
RESTORIS PST Straight Shell Inserter An impactor is a reusable instrument designed for use by orthopedic surgeons…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 24, 2014
Additional devices identified in new FSN MA-FCO 83000190: QLAB versions 10.0 with a2DQ and/or aCMQ plug-ins installed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound, Inc.
3 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.