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 Jun 1, 2016

WHIN Infusion Set - 90 Huber Needle and Wing (22 ga/1in). Intravenous delivery through intravascular ports, 20 units…

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

B. Braun Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 1, 2016

PerFuse Decompression Instrument PN: 800-0541, Lot:100650. Designed to access the femoral head for decompression.

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

Biomet, Inc.

14 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 1, 2016

ABG-HM-1 Hummi Micro Draw Blood Transfer Device Product Usage: It is used for blood transfer and collection from…

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

Hummingbird Med

FDA (openFDA device enforcement)

Medical devices

Reported Jun 1, 2016

Novocastra Liquid Mouse Monoclonal Antibody Calretinin, NCL-L-CALRET-566. Intended for the qualitative identification…

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

Leica Microsystems, Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 1, 2016

Mighty Leaf Tea Company Organic Ginger Peach Iced Tea; 100/1 oz. per case Item number 60001. UPC: 00656252600019

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

Mighty Leaf Tea

FDA (openFDA food enforcement)

Medical devices

Reported Jun 1, 2016

RayStation Therapy Treatment Planning System Stand-alone Software 3.0, 3.5, 4.0, 4.5 and 4.7., designed for treatment…

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

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Medical devices

Reported Jun 1, 2016

3.2 mm Three-fluted drill bit, sterile, Catalog ID # 03.010.060S Product Usage: Usage: The 3.2 mm Three-fluted Drill…

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

Synthes (USA) Products LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 25, 2016

Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended for the qualitative and…

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

Diamedix Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 25, 2016

Lumenis M22 System Model Number: GA-0005400 (M22 IPL + YAG Module) with Acne Filter (KT-1014971).

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

Lumenis Ltd.

FDA (openFDA device enforcement)

Food

Reported May 25, 2016

Colby Jack cheese, 8 oz. and 16 oz, Vacuumed plastic pouches

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

Msu Dept Of Fd Sci Dairy Plant

FDA (openFDA food enforcement)

Food

Reported May 25, 2016

Phosphoric Acid, 75% and 85% Food Grade (Brand Name PRAYPHOS PPA 75% FG and PRAYPHOS PPA 85% FG)

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

Prayon Inc.

FDA (openFDA food enforcement)

Food

Reported May 25, 2016

Royal Snacks Jalapeno Pistachio Royal Size

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

Royal Snacks Inc.

FDA (openFDA food enforcement)

Food

Reported May 25, 2016

Sugarfina Chocolate Malt Balls UPC Code 840278113565 SKU K1159

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

Sugarfina, LLC

FDA (openFDA food enforcement)

Medical devices

Reported May 18, 2016

Direct Drive Clip Applier CA090, indicated for ligation of tubular structures or vessels in laparoscopic and general…

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

Applied Medical Resources Corp.

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2016

Arctic Sun Temperature Management System, 5000, 100-120V and 220-240V The product is a thermal regulating system…

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

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2016

Battery Pack Used with the Capnostream"20 and Capnostream"20p Patient Monitor, Battery Packs Model Number - 016400,…

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

Medtronic

2 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported May 18, 2016

Dryses Aluminum Chlorohydrate Antiperspirant Solution, 3.4 fl. oz (100 mL) bottle, over the counter, Manufactured by…

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

Sesderma, SL

9 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported May 18, 2016

Ellipse ICD (Implantable Cardioverter Defibrillator) Model CD2411-36Q, CD2411-36C, CD1411-36Q, CD1411-36C Product…

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

St Jude Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 11, 2016

TLC¿ Self Retaining Retractor System Contents 1-RETRACTOR FRAME 6-ELASTIC STAYS STERILE EO Rx ONLY Product Usage:…

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

Applied Medical Technology Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 11, 2016

Dialog+ Hemodialysis machines: Dialog A + HE/BIC Product Code 710200L Serial # >200318 and < 2039222 The Dialog+ can be…

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

B Braun Medical Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 11, 2016

Emerald 100 Calorie Packs of Cashew Halves & Pieces, roasted and salted. 7 pack/ 0.62 oz. each (17.5 g). Ingredients:…

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

Diamond Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 11, 2016

Poly-bags containing splint strap labeled with "Pediatric" sticker. Each strap kit contains adjustable length leg…

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

Ferno-Washington Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 11, 2016

GE, Revolution CT. The system is intended for head, whole body, cardiac, and vascular X-ray Computed Tomography…

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

GE Medical Systems, LLC

FDA (openFDA device enforcement)

Food

Reported May 11, 2016

Iowa Select Herbs LLC, Acerola Berry (Malpighia), www.iowaselectherbs.com, 4 fl. Oz. (120 ml), Cedar Rapids, IA 52402

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

Iowa Select Herbs LLC

103 more products in this recall

FDA (openFDA food 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.