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.
Reported Aug 29, 2018
Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear, 8.5 Base Curve, -3.25 Power. Master Lot, containing 12…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Vision Care, Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2018
Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim urology systems facilitate radiologic and/or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Liebel-Flarsheim Company LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 29, 2018
Pasta Spinach with Cavatappi, Reser's Fine Food, item # 71117.14163, 2/4.5 # packages. UPC 0 71117 14163 4. Product is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Reser's Fine Foods, Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 29, 2018
Chocolate Gooey Brownie Ice Cream, packaged in pint-sized containers (473 mL), net wt 378 g; 1 gal. container, or 3…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Salt & Straw LLC
FDA (openFDA food enforcement)
Reported Aug 29, 2018
The Tri-Flo Subglottic Suction System
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vyaire Medical
FDA (openFDA device enforcement)
Reported Aug 29, 2018
Connecting Bolt, Model 14-442093
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 22, 2018
Rio System Irrigation Clip - Catalog # 111690 Product Usage: The RESTORIS Partial Knee Application (PKA) for use with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Aug 22, 2018
1mL Medallion Syringes Are used to inject fluids into, or withdraw fluids from the body.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 22, 2018
CDI Blood parameter monitoring system 500 H/SAT, Part No. 145883 Product Usage: The CDI System 500 provides continuous,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 22, 2018
ARCOS Modular Revision Hip System, item number 11-300814 orthopedic hip prosthesis femoral stem.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 15, 2018
Swiss Rolls***Brand Name**Swiss Rolls Chocolate (Snack) Cakes, NET WT OZ (g) PKGS***TWIN PACKS***Nutrition…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flowers Foods
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 15, 2018
Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Export For PTZ Video Ext, IP PTZ HD ErgoJust Video…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology dba Excel Tech., Ltd. (XLTEK)
FDA (openFDA device enforcement)
Reported Aug 15, 2018
Pictsweet Farms Steam'ables Baby Brussels Sprouts***NET WT 12 OZ (340g)***THIS SIDE UP IN MICROWAVE***Nutrition…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Pictsweet Company
FDA (openFDA food enforcement)
Reported Aug 15, 2018
utz Carolina Style Barbeque Potato Chips, Net Wt 2.875 OZ, UTZ Quality Foods, LLV, Hanover, PA 17301, UPC:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Utz Quality Food Inc.
FDA (openFDA food enforcement)
Reported Aug 15, 2018
AirLife Resuscitation Device, Adult labeled as the following: a. Adult, with mask, oxygen reservoir bag, Part Number…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vyaire Medical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 15, 2018
Waterpik Sonic-Fusion Professional, Model: SF-02 Product Usage: The device is composed of a unit base and an oral…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Water Pik, Inc.
FDA (openFDA device enforcement)
Reported Aug 8, 2018
VIDAS LH, Reference Numbers 30406 and 30406-01. Poduct Usage: VIDAS LH is an automated quantitative test for use on the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
FDA (openFDA device enforcement)
Reported Aug 8, 2018
PINK LEMONADE COOKIES Byrd's FAMOUS COOKIES; NET WT. 7 OZ .(198g) BOX; BYRD COOKIE COMPANY 6700 WATERS SAVANNAH, GA…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Byrd Cookie Co.
FDA (openFDA food enforcement)
Reported Aug 8, 2018
Drill (Fluted-Hard Bone), for Quattro Link 2.9mm, labeled as: a. Quattro Spade Drill, for 2.9mm, Model Number CM-9300;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cayenne Medical Inc.
FDA (openFDA device enforcement)
Reported Aug 8, 2018
1) ELITE HV, Hemostasis Valve Introducer System, Sterile EO, Rx Only, Catalog #: a) BCL-100-04; b) BCL-100-05; c)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Galt Medical Corporation
7 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2018
MAYFIELD INFINITY XR2 BASE UNIT, Part Number A2079 The MAYFIELD¿ Infinity XR2 Base Unit is intended to be used to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2018
VNS Therapy Programming System, Rx Only, Model 3000, v1.0.2.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Aug 8, 2018
XLTEK EMU40EX EEG Headbox
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology dba Excel Tech., Ltd. (XLTEK)
FDA (openFDA device enforcement)
Reported Aug 8, 2018
Nicolet¿ Ambulatory EEG
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology Inc.
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.