State

Georgia product recalls

73,576 recalls have nationwide distribution and so reach Georgia. 9,624 additional recalls listed Georgia specifically in their distribution scope.

What the numbers show

Total: 9,624
Critical: 1,474
Severe: 2,561
Most recent: 2026-10-14

Of the 9,624 recalls naming Georgia we have scored against our rubric, 1,474 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,561 (27%) are Severe.

Which agencies issued them

These figures cover only the 9,624 recalls whose distribution notice names Georgia specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26001–26025 of 83200

HighFDA (Devices)·Z-0027-2022·2021-10-13
ARTHROFOCUS Polyethylene Tibial Inserts recalled for packaging defect
Exactech is recalling ARTHROFOCUS Polyethylene Tibial Inserts due to packaging defects. Inserts lacked an oxygen barrier layer in their vacuum bag packaging, which could compromise device integrity.
Product
ARTHROFOCUS Polyethylene Tibial Inserts (Product Line: 256-12-XX, 256-13-XX). NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0055-2022·2021-10-13
Zoll ICY Intravascular Catheter Kit Recalled for Potential Tubing Leaks
ZOLL Circulation is recalling 3,425 units of the ICY Intravascular Heat Exchange Catheter Kit due to potential leaks in the catheter or start-up kit tubing. A labeling update has been issued.
Product
Zoll, REF 8700-0782-03 (IC-3893AE), ICY Intravascular Heat Intravascular Heat Exchange Catheter Kit, with central venous infusion capabilities (3 lumens), Sterile EO, Rx Only, UDI: (01)00849111050180
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0064-2022·2021-10-13
Zoll ICY Heparin Disposable Infusion Kits Recalled Due to Potential Leaks
ZOLL Circulation is recalling approximately 1,122 ICY Heparin infusion kits distributed worldwide due to potential leaks in the catheter or start-up kit tubing. No illnesses or injuries have been reported.
Product
Zoll, REF 8700-000870-40, ICY (Heparin) IVTM Disposable Pack and Start UP Kit (6 ft.), EU, New Luer
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0044-2022·2021-10-13
ZOLL COOL LINE Intravascular Catheter Kit Recalled for Potential Leaks
ZOLL Circulation is recalling COOL LINE intravascular heat exchange catheters due to potential leaks in the catheter or start-up kit tubing that could affect their function during medical procedures.
Product
ZOLL, REF 8700-0781-14 (CL-2295CO), COOL LINE Intravascular Heat Exchange Catheter kit with central venous infusion capabilities (3 lumens), HEPARIN COATED, STERILE EO, Rx Only, UDI: (01)00849111075510
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0031-2022·2021-10-13
Sleep Recording Device with Firmware Error Affecting Position Detection
Nox T3s Recorder sleep monitoring devices are being recalled due to a firmware error that causes inaccurate detection of device position, which may affect diagnostic accuracy.
Product
Nox T3s Recorder - Product Usage: intended for ambulatory recording of physiological signals during sleep.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0011-2022·2021-10-13
ELI 280 Resting Electrocardiographs Recalled Due to Device Malfunction
Welch Allyn Inc Mortara is recalling ELI 280 Resting Electrocardiographs due to device malfunction under specific operator workflows. The recall affects 14,630 units distributed nationwide and internationally.
Product
ELI, Burdick and McKesson brand 280 Resting Electrocardiographs (ELI 280, MLBUR280 and BUR280), Model Numbers: ELI280-DDB-ADAAX, ELI280-BDB-ACAAX, ELI280-CAA-AAFAD, ELI280-BDB-BDFAX, ELI280-BCB-AAAAX, ELI280-DDB-ACAAX, ELI280-DBA-BAFAX, ELI280-DCB-AAAAX…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0015-2022·2021-10-13
Paltop Scan Abutment MU devices recalled for manufacturing tolerance deviations
Paltop Advanced Dental Solutions is recalling 337 Scan Abutment MU devices due to manufacturing tolerance deviations in orientation and sizing that may delay dental restoration procedures.
Product
Scan Abutment MU, Cat. No. 30-70103 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a digital registration of an implant or abutment platform. The Paltop Advanced Dental Solutions Implant System is indicated for use in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0051-2022·2021-10-13
Zoll QUATTRO Intravascular Heat Exchange Catheter Kit Labeling Update for Leak Risk
ZOLL is issuing a labeling update for the QUATTRO Intravascular Heat Exchange Catheter Kit (188 units) addressing potential leaks from the catheter or start-up kit tubing.
Product
Zoll REF: 8700-0783-14 (IC-4593CO), QUATTRO Intravascular Heat Exchange Catheter Kit with central venous infusion capabilities (3 lumens), HEPARIN COATED, Sterile EO, Rx Only, UDI: (01)00849111075534
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0058-2022·2021-10-13
Zoll Quattro IVTM Disposable Pack and Start UP Kit Potential Leak Hazard
ZOLL Circulation is updating product labeling for Quattro IVTM disposable packs and start-up kits due to potential leaks from catheter or tubing components. Distribution includes US nationwide and international markets.
Product
Zoll, REF 8700-000766-01, Quattro IVTM Premium Disposable Pack and Start UP Kit (6 ft.)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0061-2022·2021-10-13
Zoll Quattro IV Disposable Packs and Kits Recalled for Potential Leaks
ZOLL Circulation is addressing potential leaks in Quattro IV Disposable Packs and Start-Up Kits through a labeling update affecting 334 bundles distributed worldwide.
Product
Zoll, REF 8700-000867-01, Quattro IVTM Disposable Pack and Start UP Kit (6 ft.)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0036-2022·2021-10-13
CardioQuip Cooler-Heater Device Lacks Water-Quality and Inspection Guidance
FDA recalls 1,380 CardioQuip Modular Cooler-Heater 1000(i) devices worldwide due to labeling missing guidance on water-quality maintenance and device inspection procedures.
Product
CardioQuip, Modular Cooler-Heater 1000(i), Standard Unit, Model: MCH-10RMS, CE 2797, UDI: (01) 00860000846127
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0069-2022·2021-10-13
CardioQuip Modular Cooler-Heater Units Recalled for Bacterial Water Contamination
CardioQuip heater-cooler refrigeration modules used in operating rooms could develop bacterial contamination in water systems, potentially exposing patients to infection during surgery.
Product
CardioQuip, Modular Cooler-Heater 1000(i), Refrigeration Module, Model: MCH-10RMS, UDI: (01)00860000846127 used with heat exchange devices.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0072-2022·2021-10-13
ARCH Leg Positioning System recalled due to locking pin engagement failure
Innovative Orthopedic Technologies is recalling the ARCH Leg Positioning System due to manufacturing defects that prevent locking pins from properly engaging under load.
Product
ARCH Leg Positioning System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0054-2022·2021-10-13
Zoll COOLINE Intravascular Catheter Kit recalled for potential leak hazard
ZOLL Circulation is recalling the COOLINE Intravascular Heat Exchange Catheter Kit due to potential leaks from the catheter or start-up kit tubing. 2,833 units are affected globally.
Product
Zoll, REF 8700-0781-03 (CL-2295AE), COOLINE Intravascular Heat Intravascular Heat Exchange Catheter Kit, with central venous infusion capabilities (3 lumens), Sterile EO, Rx Only, UDI: (01)00849111050173
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0025-2022·2021-10-13
Knee replacement system inserts recalled for missing oxygen barrier in packaging
Exactech is recalling knee implant system inserts that were packaged in vacuum bags lacking an oxygen barrier layer. This packaging defect may compromise product sterility and integrity.
Product
OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0074-2022·2021-10-13
ATTUNE Revision Tibial Augment recalled for packaging with incompatible screws
ATTUNE Revision Tibial Augment (5mm) packaging may include incompatible screws, potentially delaying surgery. Distributed to 10 US states.
Product
ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee joint replacement Part Code:152307001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0045-2022·2021-10-13
ZOLL COOL LINE Catheter Kit recalled for potential tubing leaks
ZOLL has recalled its COOL LINE Intravascular Heat Exchange Catheter Kit due to potential leaks in catheter and tubing components, affecting approximately 6,395 units distributed worldwide.
Product
ZOLL, REF 8700-0781-40 (CL-2295AE), COOL LINE Intravascular Heat Exchange Catheter Kit with central venous infusion capabilities (3 lumens) HEPARIN COATED, STERILE EO, Rx Only, UDI: (01)00849111075213
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0024-2022·2021-10-13
Vantage Total Ankle System Recalled for Inadequate Packaging Barriers
Exactech recalls Vantage Total Ankle System components due to vacuum-sealed packaging lacking an oxygen barrier layer, which could allow oxidative degradation of polyethylene inserts over time.
Product
Vantage Total Ankle System including a. Vantage Fixed-Bearing Polyethylene Liner Component (Product Line: 350-21-XX, 350-22-XX); b. Vantage Mobile-Bearing Polyethylene Liner Component (Product Line: 350-41-XX, 350-42-XX). NOTE: Information reflects Exactech recall…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0048-2022·2021-10-13
Zoll QUATTRO Intravascular Heat Exchange Catheter Kit Recall for Potential Leaks
Zoll Circulation recalls approximately 20,475 QUATTRO intravascular heat exchange catheter kits distributed worldwide due to potential leaks from the catheter or start-up kit tubing.
Product
Zoll REF: 8700-0783-01 (IC-4593), QUATTRO Intravascular Heat Exchange Catheter Kit Custom Luer Applause Heparin, Sterile EO, Rx Only, UDI: (01)00849111075282
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0062-2022·2021-10-13
ZOLL Solex 7 IV Disposable Kit Recalled for Potential Catheter and Tubing Leaks
ZOLL Circulation, Inc. is recalling the Solex 7 IV Disposable Pack and Start UP Kit due to potential leaks in catheter and tubing components. The Class II recall affects 79 bundles distributed worldwide.
Product
Zoll, REF 8700-000868-01, Solex 7 IVTM Disposable Pack and Start UP Kit (6 ft.)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0066-2022·2021-10-13
Zoll SOLEX 7(Heparin) IVTM Kit Recall: Potential Catheter and Tubing Leaks
ZOLL Circulation is recalling 322 bundle kits of SOLEX 7(Heparin) IVTM Disposable Pack and Start UP Kit due to potential leaks in the catheter or start-up kit tubing. The affected kits have been distributed worldwide.
Product
Zoll, REF 8700-000872-40, SOLEX 7(Heparin) IVTM Disposable Pack and Start UP Kit (6 ft.), EU, New Luer
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0003-2022·2021-10-13
Medtronic Insertion Kits Recalled for Incorrect Guidewire Label Mix-Up
Medtronic is recalling 168 Bio-Medicus Insertion Kits because a label mix-up resulted in incorrect guidewires being packaged in both model types. The mislabeling could lead to use of the wrong component during insertion procedures.
Product
Medtronic Bio-Medicus Insertion Kits, Model number 96553, Pediatric Insertion Kit, Sterile; and Model number 96551, Venous Insertion Kit, Sterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0060-2022·2021-10-13
Zoll ICY IV Disposable Pack Recall: Potential Catheter and Tubing Leaks
ZOLL Circulation recalls the ICY IV Disposable Pack and Start UP Kit due to potential leaks in the catheter or start-up kit tubing. The recall affects 42 bundles distributed worldwide.
Product
Zoll, REF 8700-000866-01, ICY IVTM Disposable Pack and Start UP Kit (6 ft.)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0053-2022·2021-10-13
ZOLL QUATTRO Intravascular Catheter Kit Labeling Update for Potential Leaks
ZOLL Circulation is updating labeling for its QUATTRO Intravascular Catheter Kit due to potential leaks from the catheter or start-up kit tubing. The update affects 1,733 units distributed worldwide.
Product
Zoll, REF: 8700-0783-03 (IC-4593AE) QUATTRO Intravascular Heat Exchange Catheter Kit, with central venous infusion capabilities (3 lumens), Sterile EO, Rx Only, UDI: (01)00849111075305
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0057-2022·2021-10-13
ZOLL ICY Intravascular Catheter Kit Recalled for Potential Catheter and Tubing Leaks
ZOLL Circulation is recalling its ICY Intravascular Heat Exchange Catheter Kit due to potential leaks from the catheter or start-up kit tubing. The recall affects 58 kits distributed worldwide.
Product
Zoll, REF 8700-0657-40 (IC-3893AE), ICY Intravascular Heat Intravascular Heat Exchange Catheter Kit, with central venous infusion capabilities (3 lumens), Heparin, Sterile EO, Rx Only, UDI: (01)00849111075107
Category
Medical Device
Distribution
Distributed nationwide