State

Georgia product recalls

73,741 recalls have nationwide distribution and so reach Georgia. 9,632 additional recalls listed Georgia specifically in their distribution scope.

What the numbers show

Total: 9,632
Critical: 1,471
Severe: 2,565
Most recent: 2026-10-28

Of the 9,632 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 2,565 (27%) are Severe.

Which agencies issued them

These figures cover only the 9,632 recalls whose distribution notice names Georgia specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

37476–37500 of 83373

HighFDA (Devices)·Z-1885-2019·2019-07-03
GE Healthcare Recalls Centricity PACS-IW Universal Viewer Software
GE Healthcare is recalling Centricity PACS-IW with Universal Viewer version 5.0 because medical images may be missing without warning.
Product
Centricity PACS-IW with Universal Viewer version 5.0, Model Number 2068177-001 Product Usage: Centricity Universal Viewer is a device that displays medical images and data from various imaging sources, and from other healthcare information sources. Medical images and data…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1853-2019·2019-07-03
Maquet VOLISTA Surgical Lights Recalled for Coating Crack Risk
Maquet is recalling 11 VOLISTA StandOP Surgical Lights because coating on the light head forks may crack, posing a risk of particles falling into the surgical field.
Product
Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811910 Model:VLT600SF STP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1878-2019·2019-07-03
GE Healthcare Recalls ECG Leadwire Sets Due to Defibrillation Risk
GE Healthcare is recalling specific ECG leadwire sets because they may reduce energy delivery during defibrillation, potentially limiting the success of the procedure.
Product
Leadwire sets with snap ends: REF/Catalog Number Description 2106381-001 ECG Leadwire set, 5-lead, snap, AHA, 74 cm/ 29 in 2106381-002 ECG Leadwire set, 5-lead, snap, AHA, 130 cm/ 51 in 2106381-003 ECG Leadwire set, 5-lead, snap, IEC, 74 cm/ 29 in 2106381-004 ECG Leadwire…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1857-2019·2019-07-03
Maquet VOLISTA Surgical Lights Recalled for Coating Crack Risk
Maquet is recalling two VOLISTA StandOP Surgical Lights because the light head coating may crack, posing a risk of particles falling into the surgical field.
Product
Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229000A Model: VST60SF AIM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1873-2019·2019-07-03
Thermo Scientific General Purpose Dynamic Bath Recalled for Assembly Error
Thermo Fisher Scientific is recalling two Thermo Scientific General Purpose Dynamic Bath units due to an assembly error that may cause the fluid temperature to rise above the user's set point.
Product
Thermo Scientific General Purpose Dynamic Bath Precision 5L GP Bath Model Number: TSGP05
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-1858-2019·2019-07-03
Maquet VOLISTA Surgical Lights Recalled for Coating Crack Risk
Maquet is recalling six VOLISTA StandOP Surgical Lights because the coating on the light head forks may crack, posing a risk of particles falling into the surgical field.
Product
Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229001A Model: VST60DF AIM
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·19E044000·2019-07-03
DLT Recalls CravenSpeed Fiat Short Shifter Shafts for Breakage Risk
DLT, LLC is recalling CravenSpeed Fiat Short Shifter shafts for 2011-2019 Fiat 500 vehicles because improper manufacturing may cause the shaft to break, increasing crash risk.
Product
FIAT — FIAT 500
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·19158·2019-07-03
Nature's Truth Recalls Wintergreen Essential Oil for Child-Resistant Closure Failure
Nature's Truth is recalling wintergreen essential oil because the bottles do not meet child-resistant closure requirements, posing a poisoning risk to young children.
Product
Nature's Truth wintergreen essential oil
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1866-2019·2019-07-03
Thermo Fisher Isotemp Water Bath Recalled for Assembly Error
Thermo Fisher Scientific is recalling five Isotemp 10L General Purpose Water Baths due to an assembly error that may cause the fluid temperature to rise above the set point.
Product
Fisher Scientific Isotemp -General Purpose Water Bath: lsotemp 10L GP Bath Model Number: FSGPD10
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-1868-2019·2019-07-03
Thermo Scientific General Purpose Dynamic Bath Recalled for Assembly Error
Thermo Fisher Scientific is recalling 12 General Purpose Dynamic Bath units due to an assembly error that may cause the fluid temperature to exceed the user's set point.
Product
Thermo Scientific General Purpose Dynamic Bath Precision 10L GP Bath Model Number: TSGP10
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-1890-2019·2019-07-03
Ethicon ENSEAL X1 Curved Jaw Tissue Sealer Recalled for Bleeding Risk
Ethicon Endo-Surgery Inc is recalling ENSEAL X1 Curved Jaw Tissue Sealers due to reported intraoperative bleeding.
Product
Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 45cm Shaft PRODUCT CODE: NSLX145C
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1882-2019·2019-07-03
Medtronic Hancock II Mitral Bioprosthesis Recalled for Incorrect Size Labeling
Medtronic is recalling 15 Hancock II T510 Mitral Bioprosthesis valves because they were mislabeled with an incorrect size. The actual valves are larger than indicated on the packaging.
Product
Hancock II T510 Bioprosthesis, Mitral, REF T505U227 - Product Usage: Replacement of malfunctioning native or prosthetic aortic and/or mitral valves.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1884-2019·2019-07-03
Medtronic Hancock II T510 Bioprosthesis Recalled for Incorrect Size Labeling
Medtronic is recalling 15 Hancock II T510 Bioprosthesis mitral valves because they were mislabeled with an incorrect size. The actual valves are larger than indicated on the packaging.
Product
Hancock II T510 Bioprosthesis, Mitral, REF T510C27 - Product Usage: Replacement of malfunctioning native or prosthetic aortic and/or mitral valves.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1431-2019·2019-07-03
Pramipexole Dihydrochloride Tablets Recalled for GMP Deviations and Cross-Contamination Risk
American Health Packaging is recalling Pramipexole Dihydrochloride Tablets due to cleaning procedure failures that may have caused cross-contamination.
Product
Pramipexole Dihydrochloride Tablets, 0.125 mg, 30 Tablets (6 tablets per blister card), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217 NDC Blister Card: 68084-793-95; NDC Carton: 68084-793-25
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1880-2019·2019-07-03
Medtronic Mosaic 310 Bioprosthesis Recalled for Incorrect Size Labeling
Medtronic is recalling 15 Mosaic 310 Bioprosthesis mitral valves because they were mislabeled with incorrect sizes. The actual valves are larger than indicated on the packaging.
Product
Mosaic 310 Bioprosthesis, Mitral, REF 310C29 - Product Usage: Replacement of malfunctioning native or prosthetic aortic and/or mitral valves.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1891-2019·2019-07-03
Qiagen RNeasy DSP FFPE Kit Recalled Due to Contaminant
Qiagen is recalling 31 units of the RNeasy DSP FFPE Kit because a contaminant in the deparaffinization solution reduces RNA purification efficiency.
Product
RNeasy DSP FFPE Kit (48), REF 73604 - Product Usage: The RNeasy DSP FFPE Kit is a system intended for the purification of total RNA from formalin-fixed, paraffin embedded (FFPE) tissues. The product is intended to be used by professional users, such as technicians and physicians…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1881-2019·2019-07-03
Medtronic Mosaic 310 Bioprosthesis Recalled for Incorrect Size Labeling
Medtronic is recalling 15 Mosaic 310 Bioprosthesis mitral valves because they were mislabeled with an incorrect size. The actual valves are larger than indicated on the packaging.
Product
Mosaic 310 Bioprosthesis, Mitral, REF 310C31 - Product Usage: Replacement of malfunctioning native or prosthetic aortic and/or mitral valves.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1851-2019·2019-07-03
Tecan Freedom EVO 200 Laboratory Robots Recalled for Gas Spring Maintenance
Tecan US, Inc. is recalling 40 Freedom EVO 200 laboratory robots because gas springs were not always replaced within the specified interval.
Product
Freedom EVO 200 - Product Usage: It is intended for routine laboratory tasks, such as general purpose pipetting and general purpose liquid handling and robotic processes.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1883-2019·2019-07-03
Medtronic Hancock II T510 Bioprosthesis Recalled for Incorrect Size Labeling
Medtronic is recalling 15 Hancock II T510 Bioprosthesis valves because they were mislabeled with an incorrect size. The actual valves are larger than indicated on the packaging.
Product
Hancock II T510 Bioprosthesis, Mitral, REF T510C27 - Product Usage: Replacement of malfunctioning native or prosthetic aortic and/or mitral valves.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1432-2019·2019-07-03
Pramipexole Dihydrochloride Tablets Recalled for GMP Deviations and Cross-Contamination Risk
American Health Packaging is recalling Pramipexole Dihydrochloride Tablets due to GMP deviations and possible cross-contamination from cleaning failures.
Product
Pramipexole Dihydrochloride Tablets, 0.25 mg, 100 Tablets (10 x 10), Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217 NDC Blister Card: 68084-440-11; NDC Carton: 68084-440-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1875-2019·2019-07-03
GE Healthcare Recalls ECG Trunk Cables Due to Defibrillation Risk
GE Healthcare is recalling ECG trunk cables that may reduce energy delivery during defibrillation, potentially limiting the success of the procedure.
Product
ECG Trunk Cables: REF/Catalog Number Description 2106305-001 ECG Trunk Cable, 3/5-lead, AHA, 3.6 m/12 ft. 2106305-002 ECG Trunk Cable, 3/5-lead, AHA, 1.2 m/4 ft. 2106305-003 ECG Trunk Cable, 3/5-lead, IEC, 3.6 m/12 ft. 2106305-004 ECG Trunk Cable, 3/5-lead, IEC, 1.2 m/4…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·19V508000·2019-07-02
Altec Recalls 2018-2019 Aerial Devices Due to Fastener Failure Risk
Altec is recalling 2018-2019 aerial devices because high-strength fasteners securing the pedestal to the turntable may fail, increasing the risk of injury or death.
Product
ALTEC — ALTEC AERIAL DEVICE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V510000·2019-07-02
Volvo Trucks Recalls 2019-2020 Models for Transmission Air Tank Strap Defect
Volvo Trucks is recalling 2019-2020 VAH, VHD, VNL, and VNR vehicles because over-tightened transmission air tank straps may deform and detach, creating a road hazard.
Product
VOLVO — VOLVO VNL, VHD, VNR, VAH
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V507000·2019-07-02
Mercedes-Benz and Freightliner Sprinter Vehicles Recalled for Rear Window Safety Glass
Daimler Vans USA is recalling 2018-2019 Mercedes-Benz and Freightliner Sprinter vans because rear side windows may be single-pane instead of laminated safety glass.
Product
MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 1500, SPRINTER 2500, SPRINTER 4500, SPRINTER 3500
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V509000·2019-07-02
Volvo Trucks Recalls 2018-2020 Models Due to Transmission Fuse Defect
Volvo Trucks is recalling 2018-2020 VAH, VHD, VNL, and VNR models because a fuse may blow, preventing the transmission from shifting and increasing crash risk.
Product
VOLVO — VOLVO VAH, VNR, VHD, VNL
Category
Vehicle
Distribution
Distributed nationwide