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 May 25, 2022
Prevantics swabs and/or swabsticks contained inside the following Aligned Medical Solutions convenience kits with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Windstone Medical Packaging, Inc.
FDA (openFDA device enforcement)
Reported May 18, 2022
The following first aid kits and cabinets containing components Medi-First XS Non-Aspirin, Product #80450, 2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Certified Safety Mfg Inc.
FDA (openFDA device enforcement)
Reported May 18, 2022
1 Series CX phototherapy units equipped with Daavlin's ClearLink Control System software versions v3.03h and 3.04v.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Daavlin Distributing Company
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 18, 2022
Bwell Bird's Nest Beverage Pandan Flavor NET 8.45 FL OZ (250mL) UPC 8373726342 24 bottles per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eastland Food Corporation
5 more products in this recall
FDA (openFDA food enforcement)
Reported May 18, 2022
Medtronic IN.PACT Admiral, Paclitaxel-coated PTA Balloon Catheter, Sterile EO, Rx Only for the following model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Vascular, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 18, 2022
Accula SARS-CoV-2 Test, REF: COV4100
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mesa Biotech, Inc.
FDA (openFDA device enforcement)
Reported May 18, 2022
OnGuard2 CSTD Bag Adaptor SP A Chemfort CSTD Product, Product code MG412143
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Simplivia Healthcare Ltd.
FDA (openFDA device enforcement)
Reported May 18, 2022
Oral Rapid SARS-CoV-2 Antigen Rapid Test Kit; COVID 19 Test
High riskUsing this product could cause serious injury, illness or death — stop using it now.Woodside Acquisitions Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 11, 2022
WHOLE FOODS MARKET red lentil dal NET WT. 12 OZ (340g) DISTRIBUTED BY: WHOLE FOODS MARKET AUSTIN, TX 78703 UPC 1 95515…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bakkavor Foods USA Inc.
FDA (openFDA food enforcement)
Reported May 11, 2022
TRAY RING COVER, REF OM271000, CONTAINS (1) TRAY RING COVER, STERILE R, Rx Only,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Surgical Vision Inc.
FDA (openFDA device enforcement)
Reported May 11, 2022
Atellica IM Enhanced Estradiol (eE2) 100T - In vitro diagnostic use in the quantitative determination of estradiol SMN:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 11, 2022
Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold); COVID 19 Test
High riskUsing this product could cause serious injury, illness or death — stop using it now.SML Distribution, LLC
FDA (openFDA device enforcement)
Reported May 6, 2022
Pop’s Que and Stew Recalls Frozen Stew Products Produced Without the Benefit of Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pop’s Que and Stew
USDA FSIS
Reported May 4, 2022
ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carl Zeiss Meditec AG
FDA (openFDA device enforcement)
Reported May 4, 2022
Kinder Happy Moments Kinder Chocolate and Crispy Wafers Assortment 14.1 OZ (400g) square box with lid. Best by: July…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ferrero USA Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 4, 2022
Empower Introducer Sheath with Hydrophilic Coating 21F x 56cm Model: 668782-100 (US)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Freudenberg Medical, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 4, 2022
da Vinici X da Vinci Xi Sureform 45 REF 480445 da Vinci X da Vinci Xi Sureform 45 Curved-Tip REF 480545 da Vinici X da…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported May 4, 2022
MEDTRONIC INTERSTIM THERAPY SYSTEM FOR URINARY CONTROL, which includes the following: a) Handset with Communicator,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported May 4, 2022
Rebel Pistachio Ice Cream, one pint (473 mL, UPC 8 53149 00821 1, Manufactured by Rebel Creamery LLC, Midway, UT 84049.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rebel Creamery
FDA (openFDA food enforcement)
Reported May 4, 2022
RocheDiabetes Care Platform Software version 2.5.2 material number 08888353001. This is a web application software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported May 4, 2022
IMMULITE 2000 Systems HCG [200 Tests, material number 10381206, catalog number L2KCG] and [600 Tests, material number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported May 4, 2022
TearCare version 1.0 SmartHubs
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sight Sciences, Inc.
FDA (openFDA device enforcement)
Reported Apr 27, 2022
4.0mm x 10mm Cannulated Screw, Short Thread; Part number 3005-40010
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 27, 2022
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow, REF H93866100, 100 slip tip caps/package.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
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.