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 48,124 notices were distributed nationwide, so they reach Georgia too — those are in the archive.

Medical devices

Reported Jul 8, 2015

Etest Cefotaxime CT 256 WW and Etest Cefotaxime CT 256 US. in vitro diagnostic.

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

BioMerieux SA

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2015

HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac transplantation in patient who are at risk of…

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

HeartWare Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2015

Dr. Sheffield's LUBRI GEL 3 oz (85 g) Non sterile over-the-counter personal lubricant.

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

Sheffield Pharmaceuticals, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2015

The Rapidlab 1260 system is a blood gas analyzer used for laboratory testing of blood gases, electrolytes, metabolites…

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

Siemens Healthcare Diagnostics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2015

Spine Wave Access Kit, Catalog Number 10-1530 Package contents: RLSP494-Rhythmlink Monopolar Stimulating Probe and…

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

Spine Wave, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2015

Infinite F500, in vitro diagnostic. Product Usage: The Tecan Infinite F500 is a multifunctional microplate reader with…

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

Tecan US, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2015

Natural Knee II Revision Femoral Stem, 125mm, item 6215-12-185. packaged in configuration 803/791. Knee Prosthesis…

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

Zimmer, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2015

BLUE BELL COUNTRY COOKIE VANILLA ICE CREAM & CHOCOLATE CHIP COOKIE SANDWICH 5.75 FL OZ (170 mL)

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

Blue Bell Creameries, LP

285 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jul 1, 2015

Diet Dr. Pepper, 8 x 12 fl. oz. PET bottle, Bottled under the authority of Dr. Pepper Company, 5301 Legacy Drive,…

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

Coca-Cola Company (The)

FDA (openFDA food enforcement)

Medical devices

Reported Jul 1, 2015

LapSac Surgical Tissue Pouch. The current intended use for the LapSac Surgical Tissue Pouch is for isolating tissue…

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

Cook Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 1, 2015

McKesson Medi-Pak Vaginal Speculum, 10/bag Reorder No. 11-8309 Used to expose interior of the vagina to facilitate…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2015

SNOBIZ CHEESECAKE SHAVE ICE FLAVOR, 10 pouches/carton; 8 cartons/case (80 pouches total per case), 104 gram per pouch,…

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

Crystal Fresh

FDA (openFDA food enforcement)

Food

Reported Jul 1, 2015

Epi breads, 7" French Hoagie Sliced, Net Weight 10.4 lbs., Lavoi Corporation, EPI Breads, 4710 West Ledbetter, Dallas,…

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

Lavoi Corporation d/b/a/ Epi De France

21 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 1, 2015

VersaTREK Instrument Series 240 REF 6240, Manufactured for Remel Inc. The VersaTREK System is for cultivating and…

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

Remel Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 1, 2015

Lifesaver Single Patient Use Manual Resuscitator Product Usage: The Hudson RCI Lifesaver Single Patient Use manual…

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

Teleflex Medical

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2015

Cambridge House Royal Smoked Salmon Sliced Side Products are packaged in Reduced Oxygen Package (ROP). Product is…

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

The Santa Barbara Smokehouse, Inc.

8 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jul 1, 2015

Chocolate covered wafers (Bocadin) in plastic packaging sold under the Mi Costenita brand and packaged and distributed…

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

Yoli, Inc. dba Mi Costenita

FDA (openFDA food enforcement)

Medical devices

Reported Jun 24, 2015

Amerigel Hydrogel Gauze Dressing 2 x 2, A5002. Wound Management.

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

Amerx Health Care Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2015

BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon Light Glove Part Number: 584569 Ophthalmic…

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

Beaver-Visitec International Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 24, 2015

Byrds Famous Cookies, Benne Bits, Net Wt. 6 oz. tins, UPC: 0-74882904651-8, Byrd Cookie Company, P.O. Box 1308,…

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

Byrd Cookie Co.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 24, 2015

HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and 1103 / OUS: 1100,1101,1102,1104,1104JP and 1205.…

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

HeartWare Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2015

ELI 380 Electrocardiograph. The ELI 380 is intended to be a high-performance, multichannel resting electrocardiograph.…

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

Mortara Instrument, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2015

CADD¿- Solis Ambulatory Infusion Pump, Model 2111 & 2112, Version 1.0, Version 2.0 and Version 3.0 & Model 2120,…

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

Smiths Medical ASD, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2015

Navigation System II-Cart, 7700-100-000 with Articulated Arm Camera, 7700-103-001 and Articulated Arm Camera,…

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

Stryker Instruments Div.

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.