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.

Medical devices

Reported May 24, 2017

Access BR Monitor, Part No. 387620

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

Beckman Coulter Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 24, 2017

ETEST ETP32 (Ertapenem) Ref. 531640, 531600, blister packaging ETEST is a quantitative technique for determining the…

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

BioMerieux SA

FDA (openFDA device enforcement)

Medical devices

Reported May 24, 2017

GIZA Vertebral Body Replacement

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

Eden Spine Europe SA

FDA (openFDA device enforcement)

Food

Reported May 24, 2017

Moondance desserts gluten free Chocolate Chip Cookie Bar 12 oz (340g) UPC 36211 68096 9

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

Moondance Heavenly Desserts, LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 24, 2017

enGen (TM) Laboratory Automation Systems using all TCAutomation(TM) Software Versions with the InOut Communication…

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

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported May 24, 2017

Navitrack¿ System - OS Knee Universal, Orthopedic Stereotaxic Instrument

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

Orthosoft, Inc. dba Zimmer CAS

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 24, 2017

Wingman 35 Crossing Catheter, 65cm, Model Numbers: WGM35065US WGM35065CE WGM35090US WGM35090CE WGM35135US WGM35135CE

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

ReFlow Medical

FDA (openFDA device enforcement)

Medical devices

Reported May 24, 2017

ADVIA Centaur Systems Insulin Calibrator; Test Code: Calibrator IRI; Catalog Number: 04618899

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 May 24, 2017

WECK Visistat 35R Disposable Skin Stapler, Ref 528135, Rx Only, Sterile EO, Visistat is indicated for the external skin…

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

Teleflex Medical

FDA (openFDA device enforcement)

Medical devices

Reported May 17, 2017

Microfil Composite Instruments are packaged in an unsealed plastic sleeve, which is then placed in a cardboard box.…

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

Almore International Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 17, 2017

Anthrex Bio-SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching

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

Arthrex, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 17, 2017

CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit and also part of the lnflatoball Pessary…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Food

Reported May 17, 2017

Reser's Fine Foods, American Classics Macaroni Salad, Net Wt 1 lb. (454 g) UPC 7117.19007, packaged in 16 oz plastic…

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

Reser's Fine Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 17, 2017

Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is a member of the Navigation portfolio and is…

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

Stryker Instruments Div.

FDA (openFDA device enforcement)

Food

Reported May 17, 2017

Vertical Pharmaceuticals OB Complete with DHA Prenatal Multivitamin, 60 softgels Rx Only, Manufactured for: Vertical…

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

Vertical Pharmaceuticals, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 10, 2017

MR GHIATAS Beaded Breast Localization Wire, Product Code: 477201, 479201 Product Usage: The GHIATAS Beaded Breast…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported May 10, 2017

Kabob's Acquisition, Inc. Recalls Meat and Poultry Products Due to Possible Listeria Contamination

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

Kabobs Aquisition, LLC

USDA FSIS

Food

Reported May 10, 2017

Hand Crafted, LG Paleteria, La Granja, Mango Flavored Ice cream, Wt. 4 oz., in clear flexible plastic wrap.

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

La Granja Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 10, 2017

Shandon Rapid Chrome Kwik-Diff Kit Part Number: 9990700 Shandon Rapid Chrome Kwik-Diff Reagent #3 Part Number 9990707…

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

Richard-Allan Scientific Company

FDA (openFDA device enforcement)

Medical devices

Reported May 10, 2017

Accu-Chek Connect Diabetes Management App versions 2.0.0, 2.0.1 and 2.1.0 for iOS and Android Product Usage: This is a…

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

Roche Diabetes Care, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 3, 2017

01.4mm x 457mm (18in) K-Wire, Threaded Blunt, Ref 9080B-18T, Qty: 1 per pack, Material: SS 316L, Full Temper, per ASTM…

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

Amendia, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 3, 2017

ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire, Part Number: 7-10026-01,Model Number: VPR-GW-FT14.…

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

Cardiovascular Systems Inc.

FDA (openFDA device enforcement)

Food

Reported May 3, 2017

Organic Marketside Spring Mix, net Wt. 5 oz. (142g) packed in rigid plastic container, UPC code 6 8113132897 5.

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

Fresh Express Incorpated

FDA (openFDA food enforcement)

Food

Reported May 3, 2017

Amish Creamery Butter Cheese Sold under the following brand names: Amish Classic 6 lb & 15 ib and Guggisberg 15 ib…

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

Guggisberg Cheese Inc.

8 more products in this recall

FDA (openFDA food 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.