State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Trader Joe's 10oz Banh Mi Style Salad w/ Tofu was recalled because it may contain Listeria monocytogenes. Consumers should stop eating the product and follow FDA recall instructions.
Fuji Food Products is recalling Trader Joe's Tofu Spring Rolls due to potential Listeria monocytogenes contamination.
Fuji Food Products is recalling Trader Joe's Smoked Salmon Philly Rolls due to potential Listeria monocytogenes contamination.
Fuji Food Products is recalling Okami 8pc Seafood Combo products due to potential Listeria monocytogenes contamination.
Trader Joes Queso Fundido 16oz is recalled due to potential Listeria monocytogenes contamination. The product was distributed in multiple states.
Lin's Waha International Corp.'s Bingtangyangmei waxberry product was recalled because it contains undeclared sulfites and cyclamates.
Northern Fisheries Ltd. is recalling 1,251 cases of frozen yellowfin tuna ground meat because it may contain increased levels of histamine, posing a risk of scombrotoxin fish poisoning.
The Okami brand 16pcs Sushi Platter (SKU 28201) was recalled because it may contain Listeria monocytogenes, a high-risk pathogen.
Axis-Shield Diagnostics is recalling 740 units of Liquid Stable 2-Part Homocysteine Reagent due to potential performance issues detected during routine testing.
Ferris Coffee and Nut Company is recalling R.H. Macy's Roasted Salted Cherries due to undeclared cashew, pecan, milk, and soy allergens.
Northern Fisheries Ltd. is recalling 1,052 cases of frozen yellowfin tuna steaks in Florida, Georgia, New York, Illinois, and Rhode Island due to potential scombrotoxin fish poisoning.
Mazor Robotics is recalling 93 Snapshot Tracker Kits because they were not manufactured to specifications, potentially causing navigational inaccuracies and patient injury.
Bard Peripheral Vascular Inc is recalling 727,034 units of the Bard Max-Core Disposable Core Biopsy Instrument due to complaints of failure to fire and failure to obtain samples.
RaySearch Laboratories is recalling RayStation software versions 4.0 through 9.0 because a bug may reset beam settings, requiring dose recalculation.
3M is recalling Durapore Advanced Surgical Tape because long-term exposure to high moisture may cause bond failure and fiber fraying, posing a risk of accidental ingestion or aspiration.
Northern Fisheries Ltd. is recalling 200 cases of frozen yellowfin tuna loins because they may contain increased levels of histamine, posing a risk of scombrotoxin fish poisoning.
Cardinal Health is correcting labeling on S.M.A.R.T. Nitinol Stent Systems that incorrectly stated they were 'MRI Safe' instead of 'MRI Conditional'.
Axis-Shield Diagnostics is recalling 740 units of Liquid Stable 2-Part Homocysteine Reagent due to potential performance issues detected during routine testing.
Ferris Coffee and Nut Company is recalling R.H. Macys & Co. Cinnamon Roasted Almonds due to an incorrect product label on the back panel.
Diagnostica Stago is recalling 5,498 units of STA Unicalibrator because a positive bias was confirmed when compared to International Standards.
Ortho Clinical Diagnostics is recalling Urine Electrolyte Diluent because the product may become unstable when stored in a 2mL cup for 7 days.
Cardinal Health is correcting labeling on Cordis Precise Nitinol Stent Systems because the instructions incorrectly stated the device was MRI Safe instead of MRI Conditional.
Spectrum Laboratory Products is recalling specific lots of Estriol Micronized USP because assay results did not meet specifications.
Cardinal Health is correcting labeling on S.M.A.R.T. stents that incorrectly stated they were MRI Safe. The correct classification is MRI Conditional.
Lifelines Neuro is recalling 12 ElectroTek Temporal Sensor Cables due to potential incorrect placement labels that could lead to improper electrode placement during EEG studies.