State

Georgia product recalls

73,827 recalls have nationwide distribution and so reach Georgia. 9,635 additional recalls listed Georgia specifically in their distribution scope.

What the numbers show

Total: 9,635
Critical: 1,471
Severe: 2,567
Most recent: 2026-11-04

Of the 9,635 recalls naming Georgia we have scored against our rubric, 1,471 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,567 (27%) are Severe.

Which agencies issued them

These figures cover only the 9,635 recalls whose distribution notice names Georgia specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53976–54000 of 83462

HighFDA (Devices)·Z-2373-2016·2016-08-17
Ivoclar Vivadent Recalls OptraPol Dental Polishing Discs Due to Breakage
Ivoclar Vivadent is recalling OptraPol polishing discs and cups because parts break away during use. The recall covers 86 units distributed in 16 states.
Product
OptraPol Polishing Discs, Rx ONLY: OptraPol Refill Cup /10: REF/Product ID 634459, OptraPol Refill Small Flame/10: REF/Product ID 634458, OptraPol Assortment: REF/Product ID 634464 --Device Listing # B106952. One step polishing system for all common dental composites and…
Category
Medical Device
Distribution
16 states
HighFDA (Devices)·Z-2353-2016·2016-08-17
Stryker S3 MedSurg Bed Fowler Control Failure Recall
Stryker is recalling S3 MedSurg Beds because CPU board failures can cause the backrest electronic controls to stop working.
Product
S3 MedSurg Bed, Model 3005. Stryker Medical
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2389-2016·2016-08-17
Synthes 2.4mm Titanium Locking Screws Recalled for Breakage Risk
Synthes (USA) Products LLC is recalling 41 units of 2.4mm Titanium Locking Screws because they can break between the head and shaft due to a thin wall design.
Product
Synthes 2.4mm Titanium Locking Screws Self-Tapping with Stardrive Recess 12mm, Synthes 2.4mm Titanium Locking Screws Self-Tapping with Stardrive Recess 12mm, Plate, Fixation, Bone, Orthopedic Devices The 2.4mm Titanium Locking Screw Self-Tapping with Stardrive Recess 12mm is…
Category
Medical Device
Distribution
17 states
HighFDA (Devices)·Z-2352-2016·2016-08-17
Ortho VITROS Estradiol Reagent Recall Due to Fulvestrant Cross-Reactivity
Ortho Clinical Diagnostics is recalling VITROS Estradiol Reagent Packs because the drug Fulvestrant causes falsely high test results in postmenopausal women.
Product
VITROS Immunodiagnostic Products Estradiol Reagent Pack, Unique Device Identifier No. 10758750005017, REF/Catalog Number/Product Code 855 2630; IVD -- Ortho-Clinical Diagnostics, Pencoed, Bridgend CF35 5PZ, UK --- The VITROS Estradiol test is performed using the VITROS Estradiol…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2390-2016·2016-08-17
Stryker Triathlon Tibial Alignment Handle Recalled Due to Weld Defect
Stryker Howmedica Osteonics is recalling 47 units of the Specialty Triathlon Tibial Alignment Handle because the secondary locking mechanism may disassociate during surgery due to a weld defect.
Product
Stryker Orthopaedics Specialty Triathlon Tibial Alignment Handle with Secondary Lock, Non-Sterile, Used to complement or replace the standard instruments used during the implantation of hip, knee, trauma and upper extremities implants
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2377-2016·2016-08-17
Stryker Recalls Triathlon Modular Handle Instruments Due to Fit Issues
Stryker Howmedica Osteonics is voluntarily recalling Triathlon Modular Handle instruments because press fit specifications were not met, potentially causing disassociation.
Product
Stryker Orthopaedics Modular Handle Triathlon Instruments, Non-Sterile, REF 6541-4-808, Lot 123, NDC M546654148080S Product Usage: Is a reusable instrument that is part of the Triathlon Primary total knee arthroplasty (TKA) system as well as the Triathlon Partial Knee…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2392-2016·2016-08-17
Hitachi Scenaria CT System Recalled for Power Supply Failure Risk
Hitachi Medical Systems America is recalling 33 Scenaria CT systems because centrifugal force may cause the power supply to fail, potentially requiring patients to be rescanned.
Product
Hitachi Scenaria Computed Tomography System Hitachi Medical Systems America, Twinsburg, OH 44087
Category
Medical Device
Distribution
15 states
ModerateFDA (Devices)·Z-2367-2016·2016-08-17
Philips Brilliance BigBore CT Systems Recalled for Software Defect
Philips is recalling eight Brilliance BigBore Oncology CT systems due to a software defect causing intermittently slow response of the Host.
Product
Brilliance BigBore Oncology Computed Tomography X-ray systems, intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
Category
Medical Device
Distribution
46 states
ModerateFDA (Devices)·Z-2382-2016·2016-08-17
Philips Brilliance iCT SP CT Scanner Software Recall
Philips is recalling 57 Brilliance iCT SP CT scanners due to software issues in versions 4.1.3 and 4.1.5 that could affect equipment performance.
Product
Brilliance iCT SP Model No. 728311; To produce cross-sectional images of the body.
Category
Medical Device
Distribution
45 states
ModerateFDA (Devices)·Z-2383-2016·2016-08-17
Philips CT Scanner Software Recall for Performance Issues
Philips is recalling Ingenuity Core CT scanners due to software issues in versions v4.1.3, v4.1.4, and v4.1.5 that could affect equipment performance.
Product
Ingenuity Core Model No. 728321; To produce cross-sectional images of the body.
Category
Medical Device
Distribution
45 states
ModerateFDA (Devices)·Z-2380-2016·2016-08-17
Philips Brilliance 64 CT Scanner Software Recall
Philips is recalling Brilliance 64 CT scanners due to software issues that could affect equipment performance.
Product
Brilliance 64 CT Model 728231; To produce cross-sectional images of the body.
Category
Medical Device
Distribution
45 states
ModerateFDA (Devices)·Z-2368-2016·2016-08-17
Philips Brilliance BigBore CT Systems Recalled for Software Defect
Philips Medical Systems is recalling 17 Brilliance BigBore CT systems due to a software defect causing intermittently slow response of the Host.
Product
Brilliance BigBore Radiology Computed Tomography X-ray systems, intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
Category
Medical Device
Distribution
46 states
ModerateFDA (Devices)·Z-2344-2016·2016-08-17
Siemens Artis Angiography Systems Recalled for Image Reproduction Failure
Siemens Medical Solutions is recalling 51 Artis zee and Artis Q angiography systems due to a software error that may cause image loss after startup.
Product
Artis zee/ zeego, Artis Q/ Q.zen, stand alone system, software controlled Model numbers: 10094135, 10094137, 10094139, 10094141, 10280959, 10848281, 10848282, 10848283, 10848353, 10848255 Artis zee / zeego and Q/ Q.zen is a family of dedicated angiography systems developed for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2384-2016·2016-08-17
Philips Ingenuity CT Software Recall for Performance Issues
Philips is recalling Ingenuity Core128 CT scanners due to software issues in versions 4.1.3, 4.1.4, and 4.1.5 that could affect equipment performance.
Product
Ingenuity Core128 Model No. 728323; To produce cross-sectional images of the body.
Category
Medical Device
Distribution
45 states
ModerateFDA (Devices)·Z-2372-2016·2016-08-17
Philips Ingenuity Core 128 CT Systems Recalled for Software Defect
Philips is recalling five Ingenuity Core 128 CT systems due to a software defect causing intermittently slow response of the Host.
Product
Ingenuity Core 128 Computed Tomography X-ray systems is intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
Category
Medical Device
Distribution
46 states
ModerateFDA (Devices)·Z-2346-2016·2016-08-17
Philips MX 16-slice CT System Software Recall for Data Integrity Issues
Philips is recalling 899 MX 16-slice CT systems due to software defects that may cause patient image mix-ups or scan interruptions.
Product
MX 16-slice whole body computed tomography X-ray system. Imaging diagnostic tool.
Category
Medical Device
Distribution
18 states
ModerateFDA (Devices)·Z-2394-2016·2016-08-17
Siemens AXIOM Artis X-Ray Systems Recalled for Cooling System Contamination
Siemens is recalling AXIOM Artis angiography systems because biomass contaminants in the cooling system may damage the pump.
Product
ARTIS ZEE AND ZEEGO, system, x-ray, angiographic AXIOM Artis, Artis zee / zeego and Artis Q/ Q.zen are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2364-2016·2016-08-17
Invacare Pediatric Flowmeter Recalled for Upside-Down Rear Scale Printing
Invacare is recalling 395 Precise Rx Pediatric Flowmeters because the rear gradation scale was printed upside down, which may cause confusion during oxygen flow monitoring.
Product
lnvacare Precise Rx Pediatric Flowmeter Model Number: IRCPF16. Packed one per carton. The lnvacare Precise Rx Pediatric Flowmeter adapts to lnvacare Concentrators for low-flow usage.The gauge has a scale printed on the front side and the back side. The front scale is the…
Category
Medical Device
Distribution
30 states
ModerateFDA (Food)·F-1875-2016·2016-08-17
Healthwise Protein Chips Recalled Due to Foreign Plastic Matter
Nutritional Resources Inc. is recalling Healthwise Protein Chips because foreign plastic was observed in the product.
Product
Healthwise, Protein Chips, Barbecue Crunch, Net Weight 1.2 ounces (34 grams), Distributed by Nutritional Resources, Inc., Grovetown, GA 30813.
Category
Food
Distribution
39 states
ModerateFDA (Devices)·Z-2405-2016·2016-08-17
Topcon Recalls PASCAL Synthesis Ophthalmic Laser Systems Due to Titration Anomaly
Topcon Medical Laser Systems is recalling 205 PASCAL Synthesis ophthalmic laser systems worldwide due to a software anomaly affecting the titration process when specific functions are used.
Product
Opthalmic: PASCAL Synthesis is an ophthalmic scanning laser system. The system can perform single shot photocoagulation as is performed conventionally.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2366-2016·2016-08-17
Philips Brilliance 64 CT Systems Recalled for Software Defect
Philips Medical Systems is recalling 318 Brilliance 64 Computed Tomography X-ray systems due to a software defect causing intermittently slow response of the Host.
Product
Brilliance 64 Computed Tomography X-ray systems is intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
Category
Medical Device
Distribution
46 states
ModerateFDA (Devices)·Z-2371-2016·2016-08-17
Philips Ingenuity Core CT Systems Recalled for Software Defect
Philips Medical Systems is recalling 29 Ingenuity Core CT systems due to a software defect causing intermittently slow response of the Host.
Product
Ingenuity Core Computed Tomography X-ray systems is intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
Category
Medical Device
Distribution
46 states
ModerateFDA (Devices)·Z-2395-2016·2016-08-17
Siemens Medical Solutions Recalls Artis Q and Q.Zen Angiography Systems
Siemens Medical Solutions is recalling Artis Q and Q.Zen angiography systems because biomass in the cooling system may damage the pump.
Product
ARTIS Q AND Q.ZEN- MODULAR ANGIOGRAPHIC SYSTEM, interventional fluoroscopic x-ray system22 AXIOM Artis, Artis zee / zeego and Artis Q/ Q.zen are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2375-2016·2016-08-17
Nobel Biocare Recalls Guided Surgery Kit Instructions for Incorrect Drill Protocol
Nobel Biocare is recalling 231 Guided Surgery Kits because the Instructions for Use contain an incorrect drill protocol. The kits are used for NobelParallel CC Implants.
Product
Instructions for Use (IFU) and Manual NobPrl CC Guided Surgery Kit Instructions for Use (IFU): "NobelGuide for NobelParallel Conical Connection", id # 2002 and Manual: Guided Surgery with NobelParallel Conical Connection", id # 79423. Article # 38072, Nobel Parallel CC Guided…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2365-2016·2016-08-17
Invacare Pediatric Flowmeter Recalled Due to Upside-Down Rear Scale
Invacare is recalling 395 Precise Rx Pediatric Flowmeters because the rear gradation scale was printed upside down, which may confuse users.
Product
Invacare Precise Rx Pediatric Flowmeter Model Number: IRCPF16 AW. Packed one per carton. The lnvacare Precise Rx" Pediatric Flowmeter adapts to lnvacare Concentrators for low-flow usage.The gauge has a scale printed on the front side and the back side. The front scale is the…
Category
Medical Device
Distribution
30 states