State
20,364 recalls have nationwide distribution and so reach Georgia. 0 additional recalls listed Georgia specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Georgia consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
Helly Hansen is recalling about 13,900 adult workwear sweatshirts and hoodies because they fail to meet federal flammability standards for clothing textiles, posing a risk of burn injuries.
The TJX Companies is recalling approximately 81,700 office chairs because the back can break or detach from the seat base when occupied, posing a fall hazard. The firm has received 12 reports of the chair back failing, including 10 reports of injuries.
Patagonia is recalling about 8,000 Infant Capilene Midweight Base Layer Sets because snaps on the bodysuit can detach, posing a choking hazard to infants. One incident of a snap detaching and being mouthed by a baby has been reported.
BMW is recalling 2020-2023 S 1000XR and 2022-2023 S 1000R motorcycles because a software update may have deactivated the front wheel lift-off assistant feature without notifying riders, increasing the risk of unexpected handling and loss of control.
Primark is recalling about 1,665 children's bamboo plates sold from October 2021 through August 2022 because they contain elevated levels of lead and formaldehyde, which are toxic if ingested by children.
Smocked Runway is recalling about 7,200 Classic Whimsy children's pajamas that fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries. Consumers should stop using the product immediately and contact the manufacturer for return instructions.
Winnebago is recalling certain Travato, Solis, and Ekko motorhomes with Suburban cooktops that may develop gas leaks due to fractured burner tubes. In the presence of an ignition source, a leak poses a fire risk.
RELiON Battery is recalling certain lots of InSight Series 48V lithium-ion batteries because they can overheat, posing thermal burn and fire hazards. The company has received five reports of overheating with no injuries reported to date.
Ouwoer Kids Bike Helmets sold on Amazon from March to November 2022 fail to meet federal safety standards and may not protect children in a crash. About 120 units are affected; no injuries have been reported.
DR Power is recalling about 2,100 PRO XL501 Chipper Shredders because the fin scroll can fail and eject metal pieces from the hopper during operation. No injuries have been reported, but the company has received six reports of metal ejection.
Active Sports is recalling CTRL Imperial Wakeboard Bindings because the binding can partially detach from the baseplate or the external mount can crack, causing users to lose balance and fall into the water. The company has received 21 reports of detachment or cracking but no injuries have been reported.
Draeger Medical is recalling 893 units of NovaStar TS Standard elbow components due to magnets that could interfere with medical devices and metallic implants.
Front steering knuckles in certain Volkswagen Atlas and Atlas Cross Sport vehicles may fracture, causing loss of vehicle control and increasing crash risk. Volkswagen will inspect and replace affected knuckles free of charge.
Draeger Medical recalls NovaStar TS Anti-Asphyxia Valves due to magnets that may interfere with implanted and non-implanted medical devices and metallic implants.
Siemens Healthcare is recalling 1,865 Atellica IM Folate 700 diagnostic kits nationwide and internationally. The kits may produce inaccurate folate test results when whole blood calibration is used instead of serum calibration.
Access Vascular is recalling HydroMID 4Fr Single Lumen Maximal Barrier Kits due to an incorrect component listed on the inner kit label. The error could lead to confusion and improper use of the device.
IBSA Pharma voluntarily recalled TIROSINT levothyroxine sodium oral solution nationwide due to subpotency concerns. Affected lots are 220416 (Exp. 10/2023) and 221053 (Exp. 4/2024).
TIROSINT (levothyroxine sodium) oral solution has been recalled nationwide by IBSA Pharma Inc. due to subpotency, with the affected medication containing less active ingredient than labeled.
Dr. Reddy's Laboratories is recalling Tacrolimus 0.5 mg capsules due to the presence of one 1 mg capsule co-mingled in affected bottles. The mismatched capsule could lead to incorrect dosing in immunosuppressed patients.
Siemens ADVIA Centaur Folate 100 test kits are recalled due to negative bias when whole blood calibration is used to test serum samples. The affected kits may produce falsely low folate results.
IBSA Pharma has recalled two lots of TIROSINT levothyroxine sodium oral solution nationwide because they contain less active ingredient than labeled. The affected lots are 220409 (expiring 10/2023) and 220956 (expiring 03/2024).
Siemens Luminos Agile Max diagnostic imaging systems recalled due to default configuration parameters allowing collision with room structures, risking serious injury to staff or patients.
IBSA Pharma Inc. voluntarily recalled specific lots of TIROSINT (levothyroxine sodium) Oral Solution nationwide due to subpotency. The affected medication contains less active ingredient than labeled.
Medline is recalling sterile oncology port access trays in which some components were not properly sterilized due to improper placement during manufacturing. Healthcare facilities should immediately discontinue use of affected units.
IBSA Pharma Inc. recalls TIROSINT (levothyroxine sodium) oral solution nationwide due to subpotent formulation containing less active ingredient than labeled.