State

Georgia product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

56101–56125 of 83468

SevereFDA (Devices)·Z-1339-2016·2016-04-20
Dexcom G5 Mobile Receiver Recall for Missing Audible Alarms
Dexcom Inc is recalling 41,925 G5 Mobile Receivers because they may fail to provide intended audible alarms or alerts to users.
Product
Dexcom G5 Mobile Receiver Receiver Part Number: MT22719 Receiver (mg/dL), Black; MT22719-PNK, Receiver (mg/dL), Pink; MT22719-BLU, Receiver (mg/dL), Blue. Intended to detect trends and track glucose patterns in persons with diabetes.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1337-2016·2016-04-20
Dexcom G4 Platinum Receiver Recall for Missing Audible Alarms
Dexcom Inc is recalling G4 PLATINUM Receivers with Share because they may fail to provide intended audible alarms or alerts.
Product
Dexcom G4 PLATINUM Receiver with Share Receiver Part Number: MT22495 Receiver (mg/dL), Black; MT22495-PNK, Receiver (mg/dL), Pink; MT22495-BLU, Receiver (mg/dL), Blue. Intended to detect trends and track glucose patterns in persons with diabetes.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1334-2016·2016-04-20
Dexcom G4 Platinum Receiver Recall for Missing Audible Alarms
Dexcom Inc is recalling G4 PLATINUM Receivers because they may fail to provide intended audible alarms or alerts to users.
Product
Dexcom G4 PLATINUM Receiver Receiver Part Number: MT20649 Receiver (mg/dL), Black; MT20649-PNK, Receiver (mg/dL), Pink; MT20649-BLU, Receiver (mg/dL), Blue. Intended to detect trends and track glucose patterns in persons with diabetes.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1026-2016·2016-04-20
Gold Medal Cincinnati Style Chili Recalled for Undeclared Milk
Gold Medal Products is recalling 4 lb jars of Cincinnati Style Chili because the label failed to declare milk as an ingredient.
Product
#2473 CINCINNATI STYLE CHILI Savory Net Wt. 4 lbs (1.8kg) UPC 0 90939 12473 1 GOLD MEDAL PRODUCTS 10700 MEDALLION DRIVE CINCINNATI, OHIO 45241
Category
Food
Distribution
16 states
SevereFDA (Food)·F-1047-2016·2016-04-20
Figi's Classic Marzipan Recalled for Unlabeled Almond Content
Figi's is recalling 8-ounce packages of Classic Marzipan because the product contains almonds that are not properly labeled on the ingredients list.
Product
Figi's Classic Marzipan, item 100-0034-200, 8 ounce
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1336-2016·2016-04-20
Dexcom G4 PLATINUM Receiver Recall for Missing Audible Alarms
Dexcom Inc is recalling G4 PLATINUM receivers because they may fail to provide intended audible alarms or alerts for diabetes patients.
Product
Dexcom G4 PLATINUM (Professional) Receiver Receiver Part Number: MT20649 Receiver (mg/dL), Black. Intended to detect trends and track glucose patterns in persons with diabetes. The G4 PLATINUM CGM System and G4 PLATINUM (Professional) CGM System use the same receiver…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1338-2016·2016-04-20
Dexcom G4 Platinum Pediatric Receiver Recall for Missing Audible Alarms
Dexcom Inc is recalling 19,586 G4 Platinum Pediatric Receivers because they may fail to provide intended audible alarms or alerts.
Product
Dexcom G4 PLATINUM (Pediatric) Receiver with Share Receiver Part Number: MT22608 Receiver (mg/dL), Black (pediatrics); MT22608-PNK, Receiver (mg/dL), Pink (pediatrics); MT22608-BLU, Receiver (mg/dL), Blue (pediatrics). Intended to detect trends and track glucose patterns in…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·16V226000·2016-04-20
StarTrans Senator II Transit Buses Recalled for Seat Separation Risk
Forest River is recalling 2016 StarTrans Senator II transit buses because seats may separate from the base frame due to bolt failure, increasing injury risk in a crash.
Product
STARTRANS — STARTRANS SENATOR II
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V227000·2016-04-20
Starcraft Bus Recalls 2015-2016 Prodigy and Quest School Buses
Forest River is recalling 2015-2016 Starcraft Prodigy and Quest school buses because seats may separate from the base frame due to bolt failure.
Product
STARCRAFT BUS — STARCRAFT BUS PRODIGY, QUEST
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1064-2016·2016-04-20
Chicken of the Sea Canned Tuna Recalled for Potential Undercooking
Tri-Union Seafoods is recalling Chicken of the Sea canned tuna due to an equipment malfunction that may have caused the product to be undercooked.
Product
Chicken of the Sea 5 Oz. Canned Chunk Light Tuna in Oil, 48 cans per case, UPC code is 0 4800000195 5
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0887-2016·2016-04-20
Morrison's Pancake Mix Recalled for Potential Metal Fragments
Morrison's Pancake Mix is being recalled because it may contain small metal fragments from a wire mesh sifter.
Product
Morrison's Pancake Mix Complete Net Wt 5 LB (2.27 kg)
Category
Food
Distribution
Distributed nationwide
HighNHTSA·16V228000·2016-04-20
Toyota 4Runner Recall for Inaccurate Load Carrying Capacity Label
Gulf States Toyota is recalling 2015-2016 Toyota 4Runners with dealer-installed accessories because the load carrying capacity label may be incorrect, potentially leading to vehicle overload.
Product
TOYOTA — TOYOTA 4RUNNER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16T005000·2016-04-20
Bridgestone Recalls Firestone and Champion Tires Due to Tread Separation Risk
Bridgestone is recalling specific Firestone and Champion tires manufactured in March and April 2016 due to inconsistent rubber coverage that may cause tread separation.
Product
TIRES recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1385-2016·2016-04-20
Synthes Recalls SYNTHECEL Dura Repair Due to Adhesion Risk
Synthes (USA) Products LLC is recalling 289 units of SYNTHECEL Dura Repair because the device may adhere to anatomical structures, posing risks if a surgeon attempts to remove it.
Product
SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Device listing number: D140596, D211012 SYNTHECEL Dura Repair is intended for use as a dura replacement for the repair of dura mater in adults.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1382-2016·2016-04-20
GE Healthcare Recalls Aisys Carestation Anesthesia Devices Due to Bolus Issue
GE Healthcare is recalling Aisys Carestation anesthesia devices due to a potential safety issue involving a momentary, self-correcting anesthetic agent bolus when using 21% oxygen.
Product
GE Healthcare, Aisys Carestation.
Category
Medical Device
Distribution
41 states
HighFDA (Devices)·Z-1381-2016·2016-04-20
GE Healthcare Recalls Aisys CS2 Anesthesia Devices Due to Bolus Issue
GE Healthcare is recalling Aisys CS2 and upgraded Aisys anesthesia devices due to a potential safety issue involving a momentary, self-correcting anesthetic agent bolus when using 21% oxygen.
Product
GE Healthcare, Aisys CS2 anesthesia..
Category
Medical Device
Distribution
41 states
HighFDA (Devices)·Z-1383-2016·2016-04-20
Synthes Recalls SYNTHECEL Dura Repair Due to Adhesion Risks
Synthes (USA) Products LLC is recalling 212 units of SYNTHECEL Dura Repair because the device may adhere to anatomical structures, posing risks if removal is attempted.
Product
SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Device listing number: D140596, D211012 SYNTHECEL Dura Repair is intended for use as a dura replacement for the repair of dura mater in adults.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1368-2016·2016-04-20
ICU Medical Recalls Diana Automated Compounding Systems Due to Volume Accuracy Issues
ICU Medical is recalling 47 Diana Automated Compounding Systems because they may not meet accuracy specifications when mixing volumes under 5ml.
Product
Diana Automated Compounding System, Final Assembly, Diana Onco Plus, Item No. CH5000, CH5000R The Diana is an automated compounding device for the accurate, safe and efficient preparation of solutions by a pharmacist prior to delivery for infusion into patient.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1372-2016·2016-04-20
Maquet Recalls HLS Set Advanced Oxygenator Tubing Packs Due to Endotoxin Risk
Maquet Cardiovascular is voluntarily recalling HLS Set Advanced oxygenator tubing packs due to a potential risk of exposure to endotoxin.
Product
HLS Set Advanced with BIOLINE Coating Custom tubing packs for the oxygenator
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1065-2016·2016-04-20
Chicken of the Sea Recalls Canned Light Tuna Due to Undercooking Risk
Tri-Union Seafoods is voluntarily recalling specific lots of Chicken of the Sea canned light tuna because an equipment malfunction may have resulted in undercooked product.
Product
Chicken of the Sea 5 Oz. Canned Chunk Light Tuna in Water, 48 cans per case, UPC code is 0 4800000245 7
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1377-2016·2016-04-20
Intuitive Surgical Recalls da Vinci S Surgical System User Manuals
Intuitive Surgical is recalling da Vinci S Surgical System user manuals because using non-approved instruments with ablation probes may increase microscopic metallic particulates.
Product
da Vinci S Surgical System (IS4000) user manual English and OUS. Product Usage: The Intuitive Surgical Endoscope Instrument Control System (da Vinci Surgical System, Model IS4000) is intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1386-2016·2016-04-20
Synthes Recalls SYNTHECEL Dura Repair Due to Adhesion Risks During Removal
Synthes (USA) Products LLC is recalling 378 units of SYNTHECEL Dura Repair because the device may adhere to anatomical structures if a surgeon attempts to remove it.
Product
SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Device listing number: D140596, D211012 SYNTHECEL Dura Repair is intended for use as a dura replacement for the repair of dura mater in adults.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1363-2016·2016-04-20
Natus Medical Recalls Medix NatalCare ST-LX Neonatal Incubators
Natus Medical is recalling Medix NatalCare ST-LX neonatal incubators because defective hinge assemblies may cause ports to detach.
Product
Medix NatalCare ST-LX Intensive Care Incubator. Neonatal incubator.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1384-2016·2016-04-20
Synthes Recalls SYNTHECEL Dura Repair Due to Adhesion Risks
Synthes (USA) Products LLC is recalling 200 units of SYNTHECEL Dura Repair because the device may adhere to anatomical structures, posing risks if removal is attempted.
Product
SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Device listing number: D140596, D211012 SYNTHECEL Dura Repair is intended for use as a dura replacement for the repair of dura mater in adults.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V229000·2016-04-20
Jaguar Recalls XF Vehicles Due to Driver Air Bag Defect
Jaguar is recalling certain 2009, 2011, 2012, and 2015 XF vehicles because the driver frontal air bag may deploy improperly, increasing injury risk.
Product
JAGUAR — JAGUAR XF
Category
Vehicle
Distribution
Distributed nationwide