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 Oct 20, 2021

Elekta Medical Linear Accelerator (EMLA), configured as follows: a. Elekta Precise Digital Accelerator; b. Elekta…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 20, 2021

Ion Flexison Biopsy Needle, 19G, Extension Range : 0-3 cm, Ref: 490104-09 and 49004-10, 5-pack, Sterile EO, Rx only,…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 20, 2021

Litehouse item 15533 Ranch dressing packaged in 1.25 oz. plastic cup with seal, 336 cups per case. It is printed on the…

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

Litehouse Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 20, 2021

ECO 85CB Lotion Ultrasound 8.5 oz 24/cs ECO 40JBC Gel Ultrasound Transmission Clr 8.5 oz BTL 24/cs ECO 40JMC Gel…

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

National Distribution & Contracting Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 20, 2021

Philips, HeartStart FR2 + Defibrillator, Model # M3860A and M3861A

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

Philips North America LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 13, 2021

REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI:…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 13, 2021

Access hsTnI High Sensitivity Troponin I, REF B52699 Access Immunoassay System REAGENT PACK

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 13, 2021

CardioQuip, Modular Cooler-Heater, Model: MCH-1000(i), CE 2797, UDI: (01)00860000846103

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

CardioQuip, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 13, 2021

Nutrifill Scleral, Hybrid, and Gas Permeable (GP) Lens Insertion Solution, Physiologic Formula, Preservative Free, 35…

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

Contamac Solutions, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 13, 2021

GEL CONDUCTOR, Description/REF: 5 LITER W/DISP/4238, 24-8.5OZ BOTTLES/4248, 5 LITER/4266, distributed by DJO, LLC / DJO…

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

Djo, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 13, 2021

Nox T3s Recorder - Product Usage: intended for ambulatory recording of physiological signals during sleep.

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

Nox Medical

FDA (openFDA device enforcement)

Food

Reported Oct 13, 2021

KALE NET WT 16 OZ (1 LB) 454g Sold under the following brand names: Baker Farms 3667 Ellenton Norman Park Road, Norman…

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

Terry and Joe Baker Farms, LLC dba Baker Farms

FDA (openFDA food enforcement)

Food

Reported Oct 13, 2021

Mr. Nut brand Dried Oleaster Net Wt: 10.6 OZ (300g). Expiration date 10/2022. UPC 0360894900.

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

Vintage Food Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 13, 2021

Zoll REF: 8700-0782-01 (IC-3893), ICY Intravascular Heat Exchange Catheter Kit, with central venous infusion…

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

ZOLL Circulation, Inc.

27 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 6, 2021

Vysis CLL FISH Probe Kit with the following components: Vysis LSI p53 SpectrumOrange/ATM, SpectrumGreen and LSI…

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

Abbott Molecular, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 6, 2021

DuoDERM Control Gel Formula Border Dressings 15x15cm (1x5pk)

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

ConvaTec, Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 6, 2021

Rc Cola 12 Oz (355 mL) packaged in an aluminum can 12 can to a pack

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

Keurig Dr Pepper

FDA (openFDA food enforcement)

Medical devices

Reported Sep 29, 2021

Access SARS CoV-2 IgG (1st IS) Assay: Access Immunoassay Systems REAGENT PACK, REF C74339 Access SARS-CoV-2 IgG (1st…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

Centricity PACS-IW with Universal Viewer - Product Usage: Is a device that displays medical images (including…

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

GE Healthcare, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube,…

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

Greiner Bio-One North America, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

CoLink Bone Graft Harvester, 8mm, Sterile, Disposable, REF G05 S1008 - Product Usage: is a general instrument intended…

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

In2bones USA, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

DLP Left Heart Vent Catheters, 16 FR. Sterile, Rx Only

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

Medtronic Perfusion Systems

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

SARS-CoV-2 Process Control (Pellet) - Product Usage: intended for use as an external, non-viable control material to…

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

Microbiologics Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

Phantom Nail System, Drill, 4.6 x 300mm, Cannulated, 3/16" Sq. Connection p28 P99-110-4630

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

Paragon 28, 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.