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 Jun 17, 2020
FilmArray BCID Panel, RFIT-ASY-0126, 30, Rx Only, CE, IVD, UDI: 00815381020086 used with the following BACT/ALERT Blood…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2020
Biomet 6.5 Cannulated Screw Tap - Bone fixation screw, Item Number: 110008466 - Product Usage: Intended for temporary…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet
21 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2020
Infinix-8000V with Catheterization Table CAT-850B or CAT-860B - Product Usage: This device is a digital…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2020
Bin Butternut Squash, Bulk, Raw Product in Bins / 4, 5lb packages in each case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coastal Sunbelt Produce Co. Inc.
FDA (openFDA food enforcement)
Reported Jun 17, 2020
Healthy Choice Pesto and Egg bowls labeled in the following ways: 1) (for the US market) Healthy Choice Power Bowls…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConAgra Foods, Inc.
FDA (openFDA food enforcement)
Reported Jun 17, 2020
RadiForce GX560 monochrome LCD monitor, models 0FTD2347 and 0FTD2379 - Product Usage: is indicated for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eizo Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2020
Ovation iX Abdominal Stent Graft Systems, REF: TV-AB2080-I, TV-AB2080-J, TV-AB2380-I, TV-AB2380-J, TV-AB2680-I,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Endologix, Inc.
FDA (openFDA device enforcement)
Reported Jun 17, 2020
Genicon GENILook Model 200-005-151, 5mm diameter, 100mm length (one cannula, threaded) - Product Usage: The universal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Genicon, Inc.
13 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2020
Triever20 Aspiration Guide Catheter a component of FlowTriever Retrieval/ Aspiration System, UDI: 00850291007079
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Inari Medical
FDA (openFDA device enforcement)
Reported Jun 17, 2020
STAINLESS STEEL REPROCESSING TRAY, 8MM ENDOSCOPE, IS4000, Model No. 400498-02 - Product Usage: is designed to enable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2020
Mazor X Surgical System Positioner Type II, REF: ASM0214-02
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Jun 17, 2020
Ormco Damon Q2 Orthodontic Metal Bracket, Part No. 491-9834, L3R Hi Tq Hook, Tq +13 degrees, Rx. Manufactured by Ormco…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ormco/Sybronendo
FDA (openFDA device enforcement)
Reported Jun 17, 2020
Infant/Child Reduced Energy Defibrillation Electrodes, Part Number: 3202380-006, for use with LIFEPAK 1000…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2020
RayStation 4.0 to RayStation 5 Service Pack 2 - Product Usage: For radiation therapy and medical oncology which can…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
14 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2020
ADVIA Chemistry Fructosamine Reagent (FRUC), Siemens Material Number 10361941, UDI Number 00630414558073 - Product…
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 Jun 17, 2020
Model Number: 06917259001 UDI: 04015630976010 - Product Usage: The System s intended use environment includes anatomic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventana Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Jun 10, 2020
Power supply provided with Afinion 2, Catalog numbers 1116553, 1116554, 1116556, 1116557, 1116597, 1116598, 1116663,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Diagnostics Technologies AS
FDA (openFDA device enforcement)
Reported Jun 10, 2020
EQUISTREAM¿ XK Long-Term Hemodialysis Catheter. REF/UDI:5913230/:(01)00801741013843; 16F
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2020
Gambro Cartridge Blood Set Prime Line - Product Usage: is intended for single use in a hemodialysis treatment using…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2020
Beckman Coulter Access Immunoassay Systems, Access Free T4 Thyroxine, REF 33880 (UDI:15099590225834) for use with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2020
Pressure Monitoring Set, C-PMS, G02838
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2020
System, Tomography Computed Emmission
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)
Reported Jun 10, 2020
Type S Extension For use with Varian, CIVCO, Prescription Only - Product Usage: Device is intended for patient…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Med Tec Inc.
FDA (openFDA device enforcement)
Reported Jun 10, 2020
OSTEOVATIONEX 2CC INJECT FORMULA. REF/UDI: 390-0002/00813845020009 - Product Usage: The product provides a bone void…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Osteomed, LLC
11 more products in this recall
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.