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 48,100 notices were distributed nationwide, so they reach Georgia too — those are in the archive.
Reported Dec 20, 2023
TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP, Model Number: LF-GP
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Dec 20, 2023
Panorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 781350. Philips Magnetic Resonance (MR)…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips North America LLC
FDA (openFDA device enforcement)
Reported Dec 20, 2023
ARTIS icono (ceiling configuration), Fluoroscopic x-ray system; Model no. 11328100
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Dec 20, 2023
Spectranetics Turbo-Elite Laser Atherectomy Catheter 2.0 RX REF 420-159 Spectranetics Turbo-Elite Laser Atherectomy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectranetics Corporation
FDA (openFDA device enforcement)
Reported Dec 13, 2023
Monarch Platform REF MON-000005-01, 100-240V- 50/60Hz 1440w
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Auris Health Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 13, 2023
BAPS SHAYONA Anjir Roll Sweet rolls made from fig and nut filling Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BAPS Shayona
12 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 13, 2023
BIOFIRE Blood Culture Identification 2 (BCID2) Panel, REF: RFIT-ASY-0147, used with Maine Molecular Quality Controls,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Dec 13, 2023
Freedom Boom models series: F110, F120, F130, F320, F330, F350, F410, and F420 with built in 42A Lightweight Spring Arm…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ihb Operations B.v.
FDA (openFDA device enforcement)
Reported Dec 13, 2023
RANDOX Total Bilirubin.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
FDA (openFDA device enforcement)
Reported Dec 13, 2023
EVO+VISIAN Implantable Collamer Lens, REF:VICM5_12.1. Phakic Intraocular lens.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Staar Surgical Company
10 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 13, 2023
STAT-Site M BHB Test Strips, used with STAT-SITE M Beta-HB Meter as an in vitro diagnostic for blood ketone values.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stanbio Laboratory, LP
FDA (openFDA device enforcement)
Reported Dec 13, 2023
Vermont Village Organic Unsweetened Apple Sauce (24oz); UPC 362401 | 084648311285
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stonewall Kitchen, LLC
FDA (openFDA food enforcement)
Reported Dec 6, 2023
BD Insyte Autoguard BC Shielded IV Catheter with Blood Control Technology 20GA X 1.00in, REF: 382533
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson Infusion Therapy Systems Inc.
FDA (openFDA device enforcement)
Reported Dec 6, 2023
Acumen IQ Sensor, REFs: AIQS6, AIQS65, AIQS6R, AIQS6R5, AIQS8, AIQS85, AIQS8R5, Rx only, Sterile EO. For use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 6, 2023
Chickpea Veggie Crisps, Net Wt. 6 1/4 oz (177.1g), UPC: 02840020646
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Frito-Lay, Inc. Headquarters
FDA (openFDA food enforcement)
Reported Dec 6, 2023
RAPIDPOINT 500e Blood Gas System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 6, 2023
Breakfast Sandwich Bacon Egg & Cheddar Croissant Net Wt. 5.25oz (149g) UPC:766375253051. Packaged in clamshell…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Coastal Companies dba Hearn Kirkwood
4 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 29, 2023
BD Alaris Pump infusion sets (Product Name, Catalog #) BD AlarisTM Pump Infusion Set Vented syringe adapter Smallbore…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2023
FilmArray TORCH REF HTFA-ASY-0104. HTFA-ASY-0104 is the BIOFIRE TORCH Base which includes barcode scanner, touch screen…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Nov 29, 2023
EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Outer box UPN# M0054242CE0.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2023
Ventlab, LLC AirFlow manual resuscitator devices with integrated manometer, multiple accessory configurations to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SunMed Holdings, LLC
8 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 22, 2023
AU/DxC AU Chemistry Transferrin REF: OSR6152 Immune complexes formed in solution scatter light in proportion to their…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Biomedical Division
FDA (openFDA device enforcement)
Reported Nov 15, 2023
Similac Probiotic Tri-Blend - 0.017oz (0.50g) packaged in foil packets. 50 foil packets per carton - 3 cartons per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA food enforcement)
Reported Nov 15, 2023
Novum IQ Syringe infusion system, Product Code 40800BAXUS
High riskUsing this product could cause serious injury, illness or death — stop using it now.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.