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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.

Medical devices

Reported Apr 22, 2015

3i T3 Non-Platform Switched Tapered Implant Rx Only; 3.25 x 8.5 - 15.0 mm Dental Implants.

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

Biomet 3i, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2015

LOW PROFILE NON-LOCK SCREW; 2.7mm x 22 mm; REF 131227222; LOT RM105E. Provides the orthopaedic surgeon a means of bone…

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

Biomet, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2015

WALLACH LL 100 cryosurgical units: LL100 Cryosurgical - Part Number 900001; LL110 with Pinned Yoke - Part Number…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 22, 2015

Culinary Masters, SCHWARMA SPICE BLEND 1/50 LB, Shelf Life: 180 days.

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

Gourmet Foods International

32 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Apr 22, 2015

Kraft Macaroni & Cheese Boxed Dinner Original Flavor, 7.25oz.,packaged in blue and yellow cardboard box. There are four…

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

Kraft Foods Group Inc.

FDA (openFDA food enforcement)

Food

Reported Apr 22, 2015

PureLife Naturals Adult Multi-Plus Multi-Vitamins & Minerals Plus Herbs, 60 Pure Caps HDPE bottle

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

ReNew Life Formulas, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Apr 22, 2015

GROUND CUMIN, Net Wt. 5 lbs (2.3 Kg), UPC 7 52186 82560 0.

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

Sahadi Fine Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 22, 2015

Talon Grasping Device, 160 cm, US endoscopy. Used for retrieval of foreign bodies, tissue specimens, stones or calculi…

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

US Endoscopy Group Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2015

Instrument Kit for use with OsteoSponge SC grafts. The Instrument Kit is used to insert OsteoSponge SC grafts to fill…

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

Bacterin International, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2015

CS 8100, CATALOG # (s): 5303045, 5311129, 5303060, 5303110 Intended to produce complete or segmented tomographic…

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

Carestream Health, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2015

Pluer-evac Sahara Chest Drainage System, S-1100-08LF, Dry Suction/Dry Seal Control, Rx Only, Teleflex Medical.

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

Teleflex Medical

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2015

VasoNova Vascular Positioning System (VPS ) G4 Console Catalog number VPS-G4C Cardiovascular: The VPS Stylet and…

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

VasoNova, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 8, 2015

Granny Smith Apples, "Granny's Best" or "Big B"; sold in 40-45 lb. cases with cardboard trays or in 3 lb. poly bags…

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

Bidart Bros.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2015

ToggleLoc; fastener, fixation, non degradable, soft tissue; Artificial Ligament Fixation Device #7 PE Ziploop Extended…

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

Biomet, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2015

Bard 100% Latex-Free Urinary Drainage Bag with Anti-Reflux Chamber and Bard EX-Lok Sampling; Product Code 154006: Lot #…

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

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 8, 2015

French Broad Chocolates, Bubbie's Almond Bar, 60g (2.1 oz) bar, with aluminum foil with polyester ribbon & paper outer…

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

French Broad Luscious Chocolates

FDA (openFDA food enforcement)

Food

Reported Apr 8, 2015

Honey & Oat Mixers ready-to-eat dry cereal sold under the market pantry brand and packaged in card stock cartons with a…

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

Gilster-Mary Lee Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2015

Medtronic Dual Chamber Temporary External Pacemaker, Model 5392. Product Usage: The temporary pacemaker is used with a…

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

Medtronic Inc. Cardiac Rhythm Disease Management

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2015

Autoject E1 Fixed needle device, Model Number AJ1310, UPC Code 384701310010 The Autoject E1 is an injector used by…

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

Owen Mumford USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2015

Computed Tomography X-ray Systems (Brilliance CT 64-channel w/Essence technology, Brilliance iCT, Brilliance iCT SP,…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 8, 2015

MR. HYDE INTENSE ENERGY PRE WORKOUT, Green Apple Natural and Artificial Flavor Dietary Supplement Net Weight 8.0 OZ…

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

ProSupps USA LLC

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2015

LIS27T - Lacrimal Intubation Set RX Only Sterile Used in various ophthalmology procedures.

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

Quest Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2015

Synthes 130 Degree Aiming Arm and 125 Degree Aiming Arm; The 130 Degree Aiming Arm and 125 Degree Aiming Arm are a part…

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

Synthes, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2015

Brand Name: Persona¿ Anterior Referencing Sizer with Locking Boom The Persona Anterior Referencing Sizer is a…

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

Zimmer, 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.