State

Georgia product recalls

72,971 recalls have nationwide distribution and so reach Georgia. 9,588 additional recalls listed Georgia specifically in their distribution scope.

What the numbers show

Total: 9,588
Critical: 1,464
Severe: 2,164
Most recent: 2026-09-09

Of the 9,588 recalls naming Georgia we have scored against our rubric, 1,464 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,164 (23%) are Severe.

Which agencies issued them

These figures cover only the 9,588 recalls whose distribution notice names Georgia specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6101–6125 of 82559

HighFDA (Food)·H-0351-2025·2025-08-06
Fresh Scottish salmon fillets processed under insanitary conditions in Georgia
Fresh Scottish Salmon Fillets sold in 50 lb boxes are being recalled because ready-to-eat fish was processed under insanitary conditions, as notified by the Georgia Department of Agriculture.
Product
Fresh Scottish Salmon Fillet, Net WT (variable weight) 50 lb brown corrugated carboard box (up to 6 fillets per box). Boxes contain ice for temperature control. Keep Refrigerated.
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-2174-2025·2025-08-06
HeartSine samaritan public access defibrillators may not deliver shocks properly
HeartSine SAM 350P, 360P and 450P public access defibrillators are being recalled because a component manufacturing issue means the device may not function properly to deliver shocks. 190,516 units affected.
Product
HeartSine SAM 350P, HeartSine SAM 360P, and HeartSine SAM 450P The HeartSine samaritan¿ PAD (Public Access Defibrillator)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2225-2025·2025-08-06
Blood EMB Levine plates may carry Listeria monocytogenes contamination
Blood/EMB Levine plates, product number R02041, are being recalled because the products may contain surface and subsurface contamination of Listeria monocytogenes. 750 units are affected.
Product
Blood/EMB, Levine 100/PK, Product Number R02041
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2221-2025·2025-08-06
Volcano Visions IVUS catheters can entangle with the guide wire
Volcano Visions Digital IVUS Catheters are being recalled following reports of catheter and guide wire entanglement during radial-to-peripheral procedures, which may require surgical removal. 233,817 units affected.
Product
Volcano Visions Digital IVUS Catheter: PV.014P (Platinum), REF:85910P; PV.014P RX, REF: 014R; and PV.018, REF: 86700, 86700J used with Instructions for use.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2216-2025·2025-08-06
SmartPath to dStream XR gradient coils may act as heat source
SmartPath to dStream for XR and 3.0T systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 294 units affected.
Product
SmartPath to dStream for XR and 3.0T Model Numbers (REF): (1) 781270, (2) 782113, (3) 782129;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2232-2025·2025-08-06
LVP dual-inlet administration sets have potential for external cassette leaks
LVP Primary Administration Sets, Dual-Inlet, Low-Sorbing, Needle-Free Port, Y-Site, are being recalled because of the potential for external cassette leaks. 19,225 units are affected.
Product
LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Y-Site (Qty 25). Product Code: SET-0013-25.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2214-2025·2025-08-06
Philips MR 7700 gradient coils may act as a heat source
MR 7700 systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 82 units are affected.
Product
MR 7700 Model Numbers (REF): (1) 782120, (2) 782153;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2207-2025·2025-08-06
Philips Ingenia 3.0T CX gradient coils may act as heat source
Ingenia 3.0T CX MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 350 units are affected.
Product
Ingenia 3.0T CX Model Numbers (REF): (1) 781271, (2) 782105;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2208-2025·2025-08-06
Philips Ingenia Ambition S gradient coils may act as heat source
Ingenia Ambition S MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 611 units are affected.
Product
Ingenia Ambition S Model Numbers (REF): (1) 781359, (2) 782108, (3) 782133 (China ONLY), (4) 782139;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2175-2025·2025-08-06
Inseego dongle kit flash drives carry outdated patient monitor software
Inseego USB8 4G Dongle Kits for the Tempus Pro Monitor are being recalled because the kit's USB flash drive contains outdated software that could revert the monitor and reintroduce a previous issue. 55 units affected.
Product
Inseego USB8 4G Dongle Kit, Part Number: 01-2298, which contains USB Flash Drive, Part Number: 43-2011. The kit is an accessory to the Tempus Pro Monitor, REF: 00-1007-R, 00-1024-R, 00-1026-R
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2234-2025·2025-08-06
LVP primary administration sets have potential for external cassette leaks
LVP Primary Administration Sets, Single Outlet Low Sorbing, are being recalled because of the potential for external cassette leaks. 35,925 units are affected.
Product
LVP Primary Administration Set, Single Outlet Low Sorbing (Qty 25). Product Code: SET-0021-25.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2206-2025·2025-08-06
Philips Ingenia 3.0T gradient coils may act as a heat source
Ingenia 3.0T MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 1,467 units are affected.
Product
Ingenia 3.0T Model Numbers (REF): (1) 781342, (2) 781377, (3) 782103;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2224-2025·2025-08-06
Strep Selective II Agar plates may carry Listeria monocytogenes contamination
Strep Selective II Agar, product number R01859, is being recalled because the products may contain surface and subsurface contamination of Listeria monocytogenes. 371 units are affected.
Product
Strep Selective II Agar, Product Number R01859
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2233-2025·2025-08-06
LVP blood administration sets have potential for external cassette leaks
LVP Blood Products Administration Sets are being recalled because of the potential for external cassette leaks. 14,280 units are affected.
Product
LVP Blood Products Administration Set Dual-Inlet, Low-Sorbing, Y-Site, Mesh Filter (Qty 20). Product Code: SET-0014-20.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0350-2025·2025-08-06
Fresh Chilean salmon fillets processed under insanitary conditions in Georgia
Fresh Chilean Salmon Fillets sold in 50 lb boxes are being recalled because ready-to-eat fish was processed under insanitary conditions, as notified by the Georgia Department of Agriculture.
Product
Fresh Chilean Salmon Fillet, Net WT (variable weight) 50 lb brown corrugated carboard box (up to 6 fillets per box). Boxes contain ice for temperature control. Keep Refrigerated.
Category
Food
Distribution
4 states
HighFDA (Food)·H-0352-2025·2025-08-06
Blue fin tuna processed under insanitary conditions in Georgia facility
Blue Fin Tuna sold in 50 lb boxes is being recalled because ready-to-eat fish was processed under insanitary conditions, as notified by the Georgia Department of Agriculture. 59 lb affected.
Product
Blue Fin Tuna, Net WT (variable weight) 50 lb brown corrugated carboard box. Boxes contain ice for temperature control. Keep Refrigerated.
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-2203-2025·2025-08-06
Philips Evolution Upgrade 3.0T gradient coils may act as heat source
Evolution Upgrade 3.0T MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 50 units are affected.
Product
Evolution Upgrade 3.0T Model Numbers (REF): (1) 782117, (2) 782143;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2209-2025·2025-08-06
Philips Ingenia Ambition X gradient coils may act as heat source
Ingenia Ambition X MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 690 units are affected.
Product
Ingenia Ambition X Model Numbers (REF): (1) 781356, (2) 782109, (3) 782138;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2198-2025·2025-08-06
CoSense sampling sets may carry residual carbon monoxide from insufficient aeration
Precision Sampling Sets for the CoSense End-Tidal Carbon Monoxide Monitor are being recalled because residual carbon monoxide may remain in the cannula filter, which may raise ETCOc scores. 2,160 units affected.
Product
Precision Sampling Set, REF: C20206 for use with the CoSense End-Tidal Carbon Monoxide Monitor
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2178-2025·2025-08-06
HarmonyAIR E-Series monitor yokes may detach from the spring arm
Dual Flat Panel Monitor accessories for HarmonyAIR E-Series Surgical Lighting Systems are being recalled because the yoke assembly may detach from the spring arm. 59 units are affected.
Product
Dual Flat Panel Monitor (DFPM) accessories for HarmonyAIR E-Series Surgical Lighting Systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2218-2025·2025-08-06
Philips MR 7700 upgrade gradient coils may act as a heat source
Upgrade to MR 7700 systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 26 units are affected.
Product
Upgrade to MR 7700 Model Number (REF): 782130;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2235-2025·2025-08-06
LVP dual Y-site administration sets have potential for external cassette leaks
LVP Primary Administration Sets, Dual-Inlet, Low-Sorbing, Needle-Free Port, Dual Y-Site, are being recalled because of the potential for external cassette leaks. 348,150 units are affected.
Product
LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Dual Y-Site (Qty 25). Product Code: SET-0032-25.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2223-2025·2025-08-06
Blood agar plates may carry Listeria monocytogenes surface contamination
Blood Agar with 5% Sheep Blood, product number R01202, is being recalled because the products may contain surface and subsurface contamination of Listeria monocytogenes. 1,552 units affected.
Product
Blood Agar,5% Sheep Blood 100/PK, Product Number R01202
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0545-2025·2025-08-06
Bicillin L-A 2.4 million unit vials recalled after particulates found
Bicillin L-A (penicillin G benzathine injectable suspension) 2,400,000 units per 4 mL is being recalled because of CGMP deviations, with particulates identified during visual inspection. 19,279 vials affected.
Product
BICILLIN L-A — BICILLIN L-A (PENICILLIN G BENZATHINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2204-2025·2025-08-06
Philips Ingenia 1.5T gradient coils may act as a heat source
Ingenia 1.5T MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 2,279 units are affected.
Product
Ingenia 1.5T Model Numbers (REF): (1) 781315, (2) 718641, (3) 781396, (4) 782101, (5) 782115, (6) 782140;
Category
Medical Device
Distribution
Distributed nationwide