All recall categories

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.

Drugs

Reported Jun 21, 2017

ESTRONE USP, packaged in a) 1g bottle (NDC: 58597-8049-2), c) 5g bottle (NDC: 58597-8049-3), d) 25g bottle (NDC:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

American Pharmaceutical Ingredients LLC

FDA (openFDA drug enforcement)

Medical devices

Reported Jun 21, 2017

VITEK¿ 2 Gram-Negative identification card (GN), IVD, REF 21341, 20 cards per carton.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biomerieux Inc.

186 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 21, 2017

Chocolate chip cookie dough larabars, 10 count , UPC 100-21908-49031 incorrectly packaged in peanut butter cookie…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

General Mills, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 21, 2017

Pointe Scientific Hitachi Total Bilirubin Rl Reagent Product Usage: Two part Chemistry Reagent Hitachi Total Bilirubin…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtest Holdings, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 21, 2017

Philips DigitalDiagnost 3.1.x X-Ray System

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Electronics North America Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 14, 2017

Beekley Medical 0-SPOT Mammography Skin Markers REF 652

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Beekley Corporation

FDA (openFDA device enforcement)

Food

Reported Jun 14, 2017

California Sun Dry Sun Dried Tomato Pesto; NET WT. 8.5 oz. (241g) glass jar; Ingredients (incorrect) Garlic, Canola…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

California Sun Dry Foods

FDA (openFDA food enforcement)

Medical devices

Reported Jun 14, 2017

Oxygen Masks, Elongated (under chin), Adult Med Conc., No Tubing, Product Code 104-E;

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ConvaTec, Inc.

17 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 14, 2017

Nexstim eXima NBS System Software version 2.2 or higher. The Nexstim Navigated Brain Stimulation System (NBS System) is…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nexstim PLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 14, 2017

Denali "Original" Moose Tracks Cheesecake, Net Wt. 18 oz (510g). Black plastic base with clear plastic dome. Back label…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

The Father's Table, LLC

FDA (openFDA food enforcement)

Meat & poultry

Reported Jun 9, 2017

Pork King Sausage, Inc. Recalls Raw Sausage Link Products Due to Misbranding and Undeclared Allergen

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Pork King Sausage, Inc.

USDA FSIS

Medical devices

Reported Jun 7, 2017

Cardinal, Digital Bariatric Scale 1) model 6876, Cap 600 and 2) model 6868 Cap 1000

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cardinal Scale Mfg Co.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 7, 2017

Adenovirus (20/11 & 2/6); 0.5 mL Catalog # 212M-15; and 7.0 mL Catalog number 212M-18 Microbiology - Analyte Specific…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cell Marque Corporation

11 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 7, 2017

Angio WorkStation (XIDF-AWS801) used in conjunction with your Infinix System (INFX-8000V;INFX-8000C;INFX-8000F

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Toshiba American Medical Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 7, 2017

AIA-PACK TPOAb CONTROL SET

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Tosoh Bioscience, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 7, 2017

Chef Pierre 10 Spinach Quiche, and 6/10 Frozen Quiche, 38 oz. packed in a paper carton, keep frozen

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tyson Foods, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 31, 2017

Ceftriaxone TX 32 US S30, Ref 412302 and Ceftriaxone TX 32 US F100, Ref 507058 ETEST is a quantitative technique for…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioMerieux SA

FDA (openFDA device enforcement)

Medical devices

Reported May 31, 2017

CSI, Orbital Atherectomy System (OAS) Saline Infusion Pump, Rx only, Part Number: 7-10014, Model Number: SIP-3000.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cardiovascular Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 31, 2017

Merge Cardio software. The firm name on the label is Merge Healthcare, Hartland, WI. Intended to be used to acquire,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Food

Reported May 31, 2017

Dip Trio Mix Homemade Gourmet Dip Mix Net Wt. 2.9 oz. Distributed by: Phoenix Food, LLC. Canton, TX 75103…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Phoenix Food, LLC

FDA (openFDA food enforcement)

Food

Reported May 31, 2017

ARTISAN-STYLE PIZZA DOUGH BALL distributed under the following sizes and Product Codes: (a) 12 OZ ARTISAN-STYLE PIZZA…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Rich Products Corp.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported May 31, 2017

Herbal Tea Variety 120 ml/pouch, 40 pouches/case

High riskUsing this product could cause serious injury, illness or death — stop using it now.

U S Deer Antlers Export & Import

FDA (openFDA food enforcement)

Meat & poultry

Reported May 25, 2017

Golden Gourmet Recalls Frozen Waffle and Turkey Sausage Products Due to Possible Listeria Contamination

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Golden Gourmet, LLC

USDA FSIS

Medical devices

Reported May 24, 2017

SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for the folding and delivering of the LI61AO, LI61AOV, or…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bausch & Lomb Surgical, Inc.

FDA (openFDA device enforcement)

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Other states

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.