State
73,718 recalls have nationwide distribution and so reach Georgia. 9,632 additional recalls listed Georgia specifically in their distribution scope.
Of the 9,632 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 2,565 (27%) are Severe.
Which agencies issued them
These figures cover only the 9,632 recalls whose distribution notice names Georgia specifically. The 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Canteen Inc. dba MG Foods is recalling 58 Fresh To You Turkey & Swiss sandwiches due to positive Listeria monocytogenes test results.
Fenwal Inc is recalling specific lots of Amicus MNC Apheresis Kits because centrifuge packs may leak blood during therapeutic procedures.
The FDA is recalling MG Foods Turkey & Swiss On a Buttery Croissant because Listeria monocytogenes was detected during environmental testing of their meat slicers.
MG Foods is recalling The Club in a Spinach Wrap due to Listeria monocytogenes detected in environmental sampling.
Becton Dickinson is recalling Martin-Lewis Agar plates because they show heavy fungal growth, which may delay the diagnosis of Neisseria infections.
Arrow International is recalling OnControl Bone Lesion Biopsy Systems because the ejector rod may not insert properly, preventing sample collection.
Target is recalling Cat & Jack Baby Heart Ears Rompers because heart-shaped graphics on the knees can detach, posing a choking hazard to children.
The Quaker Oats Company is recalling Quaker Rice Crisps Sweet Barbecue Flavor due to undeclared soy. The recall covers 4,550 bags distributed to 21 states.
Trident Seafoods is recalling frozen Pacific Salmon Burgers sold at Costco due to a metal fragment found in the product.
Playgro is recalling Clip Clop infant activity rattle toys because the abacus ring can dislodge and release small beads, posing a choking hazard to small children.
Howmedica Osteonics Corp. is recalling Specialty Triathlon TS Trial Cutting Guides because the posterior condyle may fracture during transport or surgery.
Fenwal Inc is recalling 2,466 Amicus Exchange Kits because centrifuge packs may leak blood during therapeutic procedures.
Battat is recalling B. toys Firefly Frank infant teethers sold at Target because plastic wings can detach, posing a choking hazard to young children.
ROi CPS LLC is recalling 16 Regard custom cardiovascular procedure kits because drape slits may breach the sterile barrier.
Fenwal Inc is recalling 24 units of Amicus Exchange Kits because centrifuge packs may leak blood during therapeutic procedures.
Siemens is recalling 12 Ysio X.pree digital X-ray systems because a software issue may display a previous patient's image during recovery, potentially impacting diagnosis.
Audio-Technica is recalling charging cases for ATH-CK3TW wireless headphones because they can overheat and pose a fire hazard. No injuries have been reported.
Becton Dickinson is recalling BD BBL Martin-Lewis Agar due to misformulation causing heavy fungal growth, which may delay the diagnosis of Neisseria infections.
Hologic is recalling 1,355 Panther Fusion Tube Trays because they may leak, potentially causing false positive, false negative, or invalid patient results.
Fujifilm Medical Systems is recalling Synapse PACS software because it may display incorrect patient information in the viewer or PowerJacket.
Medtronic is recalling A610 Clinician Programmer software versions 2.0.4584, 2.0.4594, 2.0.4605, and 3.0.1057 due to software errors that prevent proper copying of cycling settings and cause application crashes when reading full system event logs.
Terumo is recalling 12 sternal retractor devices because the stainless steel locking plates may fracture. The devices were distributed in eight US states.
Apotex Corp. is recalling Guanfacine Extended-Release tablets because they contain trace amounts of Quetiapine Fumarate.
Cosette Pharmaceuticals is recalling specific lots of Mometasone Furoate Topical Solution due to Current Good Manufacturing Practice (CGMP) deviations.
Gf Health Products is recalling 66 units of the Drop Arm Versamode because the front casters are incorrect. The devices were distributed in the US and internationally.