State

Georgia product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41801–41825 of 83441

HighFDA (Devices)·Z-3229-2018·2018-10-03
Philips FlexVision Monitor Ceiling Suspension Recall for Detachment Risk
Philips is recalling FlexVision Monitor Ceiling Suspensions because the monitor may detach from the actuator rotor shaft, posing a risk of injury to patients, users, and bystanders.
Product
AIIuraXperFDlO, System Code 722010 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3248-2018·2018-10-03
Swissray Medical Recalls ddR Formula B X-ray Systems for Movement and Calibration Issues
Swissray Medical is recalling 26 ddR Formula B X-ray systems in the U.S. due to potential arm movement, calibration loss, and communication loss that could cause injury.
Product
ddR Formula B X-ray System, ddR Formula B Product Usage: X-ray system used for imaging
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3213-2018·2018-10-03
Philips INTEGRIS Allura 9 Monitor Ceiling Suspension Recall
Philips is recalling INTEGRIS Allura 9 systems because the monitor ceiling suspension may detach, causing the monitor to fall and risk injury.
Product
INTEGRIS Allura 9, System Code 722018 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3237-2018·2018-10-03
Philips Medical Monitor Ceiling Suspension Recall Due to Detachment Risk
Philips is recalling 5,115 medical monitor ceiling suspensions because the monitor may detach from the actuator rotor shaft and fall, posing a risk of injury to patients, users, and bystanders.
Product
Poly C- DMCP-Visub(H3000), System Code 72238 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3262-2018·2018-10-03
Biomet Recalls HipLOC Hip Fracture Fixation System Plates Due to Fit Issues
Biomet UK Ltd. is recalling 10 units of HipLOC Hip Fracture Fixation System plates due to an undersized bore that prevents the lag screw from fitting.
Product
HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Barrel 3 Hole Plate Item Number: 2110-135-003 Product Usage: The HipLOC Compression Hip Screw may be used primarily for fixation of bone fractures. Specific indications include open reduction and internal…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3277-2018·2018-10-03
Bausch + Lomb Stellaris Elite Vit Cutter Back Cap Separation Recall
Bausch & Lomb is recalling Stellaris Elite 25 GA Vit Cutters because the back cap may separate from the cutter body.
Product
Bausch + Lomb Stellaris Elite Vision Enhancement System, 25 ga. Combined Wide-Field Elite Pack, REF SE5525WV (containing the Stellaris Elite 25 GA Vit Cutter, Model BL5628), packaged in sterile trays, 6 trays/shipper.
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-3231-2018·2018-10-03
Philips AIIura Xper F010 DR Table Recall for Monitor Detachment Risk
Philips is recalling AIIura Xper F010 DR Tables because the ceiling monitor suspension may detach, posing a risk of injury to patients and staff.
Product
AIIura Xper F010 DR Table, System Code 722022 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3267-2018·2018-10-03
Bausch + Lomb Stellaris Elite Vit Cutter Back Cap Separation Recall
Bausch + Lomb is recalling Stellaris Elite 20 GA Vit Cutters because the back cap may separate from the cutter body.
Product
Bausch + Lomb Stellaris Elite Vision Enhancement System, 20 ga. Posterior Wide-Field Elite Pack, REF SE5420W (containing the Stellaris Elite 20 GA Vit Cutter, Model BL5626), packaged in sterile trays, 6 trays/shipper.
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-3230-2018·2018-10-03
Philips FlexVision Monitor Ceiling Suspension Recall Due to Detachment Risk
Philips is recalling FlexVision Monitor Ceiling Suspensions because the monitor may detach from the actuator rotor shaft, posing a risk of injury to patients, users, and bystanders.
Product
AIIuraXperFDlO/10, System Code 722011 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3212-2018·2018-10-03
Medtronic Clip Gun Magazines Recalled for Packaging Sterility Defect
Medtronic Neurosurgery is recalling Clip Gun Magazines because the packaging sterile barrier may be compromised without visible signs.
Product
Medtronic Clip Gun Magazines are packaged in individually sealed pouches and distributed in boxes containing 5 individually pouched Clip Gun Magazine. REF CM8902, Medtronic Clip Gun Magazine, Rx only, CE 0344, STERILE EO, Rx only, Single Use
Category
Medical Device
Distribution
38 states
HighFDA (Devices)·Z-3242-2018·2018-10-03
Terumo Advanced Perfusion System Recalled for Potential Electrical Short
Terumo is recalling 47 Advanced Perfusion System units because improperly torqued screws may cause an electrical short.
Product
Terumo 100/120V AC, Advanced Perfusion System Platform (APS) for use in cardiopulmonary bypass procedures. Catalog Number 801763
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3264-2018·2018-10-03
Biomet Recalls HipLOC Hip Fracture Fixation System Plates
Biomet UK Ltd. is recalling 6 units of HipLOC System 140° Plates due to an undersized bore that prevents the lag screw from fitting through the barrel.
Product
HipLOC Hip Fracture Fixation System-Hiploc System 140¿ Plate 38 mm Barrel 4 Hole Plate Item Number: 2110-140-004 Product Usage: The HipLOC Compression Hip Screw may be used primarily for fixation of bone fractures. Specific indications include open reduction and internal…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3274-2018·2018-10-03
Bausch + Lomb Stellaris Elite Vit Cutter Back Cap Separation Recall
Bausch & Lomb is recalling Stellaris Elite 23 GA Vit Cutters because the back cap may separate from the cutter body during use.
Product
Bausch + Lomb Stellaris Elite Vision Enhancement System, 23 ga. Combined Mid-Field Elite Pack, REF SE5523MV (containing the Stellaris Elite 23 GA Vit Cutter, Model BL5627), packaged in sterile trays, 6 trays/shipper.
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-3251-2018·2018-10-03
Medtronic Visualase Thermal Therapy System Recalled for MR Thermometry Inaccuracy
Medtronic is recalling Visualase Thermal Therapy System software due to potential MR thermometry inaccuracies that may cause unaccounted thermal energy spread during laser ablation.
Product
Visualase Thermal Therapy System, Software: Visualase Software versions 3.1.1 - 3.2, Product #: 9735542
Category
Medical Device
Distribution
35 states
HighFDA (Devices)·Z-3272-2018·2018-10-03
Bausch + Lomb Stellaris Elite Vit Cutter Recall for Back Cap Separation
Bausch & Lomb is recalling Stellaris Elite Vit Cutters because the back cap may separate from the cutter body.
Product
Bausch + Lomb Stellaris Elite Vision Enhancement System, 25 ga. Posterior Mid-Field Elite Pack, REF SE5425MV (containing the Stellaris Elite 25 GA Vit Cutter, Model BL5628), packaged in sterile trays, 6 trays/shipper.
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-3260-2018·2018-10-03
Boston Scientific LATITUDE Programming System Recalled for Stimulation Risk
Boston Scientific is recalling 74 LATITUDE Programming Systems due to a potential for unintended cross-chamber stimulation in pacing devices.
Product
Model 3300 LATITUDE(TM) Programming System Product Usage - The Boston Scientific LATITUDE Programming System is intended for use in hospital and clinical environments to communicate with Boston Scientific implantable systems. The software in use controls all communication…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3215-2018·2018-10-03
Philips INTEGRIS CV Ceiling Monitor Suspension Recall for Detachment Risk
Philips is recalling INTEGRIS CV systems because the ceiling monitor suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
INTEGRIS CV, System Code 722030 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3276-2018·2018-10-03
Bausch + Lomb Stellaris Elite Vit Cutter Recall for Back Cap Separation
Bausch + Lomb is recalling Stellaris Elite Vit Cutters because the back cap can separate from the cutter body.
Product
Bausch + Lomb Stellaris Elite Vision Enhancement System, 25 ga. Combined Mid-Field Elite Pack, REF SE5525MV (containing the Stellaris Elite 25 GA Vit Cutter, Model BL5628), packaged in sterile trays, 6 trays/shipper.
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-3263-2018·2018-10-03
Biomet Recalls HipLOC Hip Fracture Fixation System Plates
Biomet UK Ltd. is recalling 44 units of the HipLOC Hip Fracture Fixation System due to an undersized bore that may prevent the lag screw from fitting.
Product
HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Barrel 4 Hole Plate Item Number: 2110-135-004 Product Usage: The HipLOC Compression Hip Screw may be used primarily for fixation of bone fractures. Specific indications include open reduction and internal…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3273-2018·2018-10-03
Bausch + Lomb Stellaris Elite Vit Cutter Recall Due to Cap Separation
Bausch & Lomb is recalling Stellaris Elite 25 GA Vit Cutters because the back cap may separate from the cutter body.
Product
Bausch + Lomb Stellaris Elite Vision Enhancement System, 25 ga. Posterior Wide-Field Elite Pack, REF SE5425WV (containing the Stellaris Elite 25 GA Vit Cutter, Model BL5628), packaged in sterile trays, 6 trays/shipper.
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-3227-2018·2018-10-03
Philips Allura Xper F010 Ceiling Monitor Suspension Recall
Philips is recalling Allura Xper F010 systems because the ceiling monitor suspension may detach, causing the monitor to fall and potentially injure patients or users.
Product
Allura Xper F010, System Code 722003 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3259-2018·2018-10-03
Boston Scientific Recalls VISIONIST X4 CRT-P Pacemakers Due to Battery Depletion
Boston Scientific is recalling VISIONIST X4 CRT-P pacemakers because hydrogen-induced accelerated battery depletion may require early replacement.
Product
VISIONIST X4 CRT-P (Cardiac Resynchronization Therapy Pacemaker)
Category
Medical Device
Distribution
48 states
HighFDA (Devices)·Z-3228-2018·2018-10-03
Philips AlluraXperFOlO/lO Ceiling Monitor Suspension Recall
Philips is recalling 5,115 AlluraXperFOlO/lO systems because the ceiling monitor suspension may detach, causing the monitor to fall and potentially injure patients or users.
Product
AlluraXperFOlO/lO, System Code 722005 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3269-2018·2018-10-03
Bausch + Lomb Stellaris Elite Vit Cutter Recall for Cap Separation
Bausch & Lomb is recalling Stellaris Elite Vit Cutters because the back cap may separate from the cutter body during use.
Product
Bausch + Lomb Stellaris Elite Vision Enhancement System, 23 ga. Posterior Mid-Field Elite Pack, REF SE5423MV (containing the Stellaris Elite 23 GA Vit Cutter, Model BL5627), packaged in sterile trays, 6 trays/shipper.
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-3233-2018·2018-10-03
Philips Allura Xper F010 DR Table Recall for Monitor Detachment Risk
Philips is recalling 5,115 Allura Xper F010 DR Tables because the ceiling monitor suspension may detach, posing a risk of injury from falling equipment.
Product
Allura Xper F010 DR Table, System Code 722014 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide