State
72,984 recalls have nationwide distribution and so reach Georgia. 9,588 additional recalls listed Georgia specifically in their distribution scope.
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 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mammut Sports Group is recalling Skywalker Pro Via Ferrata Sets because the carabiner can open without engaging the safety latch, creating a risk of serious injury or death from falls.
Endless Pools is recalling about 11,500 Manual Retractable Security Pool Covers because improper installation can leave gaps larger than 4.5 inches, posing drowning and entrapment risks to children.
Approximately 1,158,000 Anker PowerCore 10000 power banks (model A1263) are recalled because their lithium-ion batteries can overheat, creating fire and burn hazards. Anker has received 19 reports of fires and explosions, including property damage totaling over $60,700.
GM is recalling certain 2019-2024 Chevrolet Silverado Medium Duty trucks because the brake pressure sensor may leak fluid into the switch and short circuit. Owners are told to park outside.
Chrysler is recalling certain 2024-2025 Dodge Charger vehicles because the amplifier may be missing software, preventing exterior sound including pedestrian warnings.
Chrysler is recalling certain 2023 Pacifica and Voyager vehicles because a manufacturing error may prevent the rearview camera image displaying, failing FMVSS 111.
TI Outdoor Power Equipment is recalling about 113,000 RYOBI 40V 24-inch cordless hedge trimmers because the blade can unexpectedly activate from pressing only one control, causing lacerations. Consumers should stop using the trimmer and return it for a free replacement.
SunMed Holdings is recalling 11,358 Adult Manual Resuscitators because the filter may be incorrectly attached to the patient port instead of the exhalation port, risking interruption or delay in patient resuscitation that could cause serious harm or death.
Publix Super Markets is recalling Greenwise Pear Kiwi Spinach & Pea Baby Food Pouches due to elevated levels of lead, cadmium, and arsenic. The product was distributed across eight southeastern states.
Pennrose Farms is recalling cucumbers due to potential Salmonella contamination. The recall affects 5-lb mesh bags distributed to FL, NJ, GA, IL, and OH.
Torrent Pharma Inc. is recalling Fluoxetine Tablets, USP, 20 mg in a 28-count carton due to the presence of N-Nitroso Fluoxetine exceeding the interim acceptable intake limit.
Silex Medical is recalling Signature Laparoscopic Atraumatic Grasper instruments (Model 5864000) due to incomplete insulation on the shaft that leaves an exposed area near the rotator wheel, posing an electrical safety risk during surgical use.
Silex Medical is recalling 8 units of Signature Laparoscopic Debakey Grasper instruments (Model 5862100) due to incomplete insulation on the shaft near the rotator wheel, which could expose the user or patient to electrical contact.
Mozarc Medical US LLC is recalling Palindrome Precision SI Chronic Hemodialysis Catheters (Sport Pack) due to a potential breach of sterile barrier packaging. Approximately 95,938 units distributed nationwide and in Canada and Mexico are affected.
Silex Medical is recalling 2 units of a Signature Laparoscopic Instruments Dolphin Nose Grasper with Rotating Shaft due to incomplete insulation on the shaft, leaving an exposed area near the rotator wheel.
Silex Medical is recalling the Signature Laparoscopic Alligator Grasper with Rotating Shaft (Model 5863050) because insulation on the tube does not fully extend to the proximal end of the shaft, leaving an exposed uninsulated area near the rotator wheel.
Mozarc Medical is recalling Palindrome Precision H Chronic Hemodialysis Catheter Sport Pack units due to a potential breach of sterile barrier packaging. The affected catheter models were distributed nationwide in the US and in Canada and Mexico.
Silex Medical is recalling 6 units of the Signature Laparoscopic Bullet Tip Grasper with Rotating Shaft due to incomplete insulation on the shaft near the rotator wheel, which could expose users to electrical hazards.
Mercedes-Benz is recalling 2023 GLC 300 and GLC 300 4MATIC vehicles because missing caps allow improper headlight adjustment, increasing crash risk.
Silex Medical recalls the Signature Laparoscopic Sharp Tooth Grasper due to incomplete insulation on the shaft near the rotator wheel, which creates an electrical hazard during use.
Dexcom G7 iOS App version 2.7.0 can enter a state where glucose readings freeze and alerts do not trigger, risking missed detection of dangerously high or low blood sugar. Other connected devices like Apple Watch and insulin pumps continue to receive glucose data directly from the transmitter.
Rivian is recalling certain 2025 R1S and R1T vehicles because one or both front turn signals may fail to illuminate and flash, failing FMVSS 108. 27,882 units affected.
Nova Bus is recalling certain 2022-2023 LFS buses because a digital display firmware error may leave the instrument panel turn signal indicators solidly lit, failing FMVSS 108.
Mozarc Medical is recalling Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Packs due to a potential breach of sterile barrier packaging that could compromise the catheter's sterility.
Silex Medical is recalling Signature Laparoscopic Instruments (Model 5881033) because insulation on the shaft does not fully extend to the proximal end, leaving an exposed area near the rotator wheel.