State
73,833 recalls have nationwide distribution and so reach Georgia. 9,635 additional recalls listed Georgia specifically in their distribution scope.
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.
LeMaitre Vascular is recalling 4,315 Over-the-Wire Embolectomy Catheters due to a manufacturing defect that may compromise packaging sterility.
Philips is recalling 1,765 Brilliance 64 CT systems worldwide due to software defects that may cause operational errors, image issues, or misdiagnosis.
Skipanon Brand Seafoods LLC is recalling approximately 57,000 cans of smoked coho salmon due to lack of documentation and possible under-processing, which could lead to Clostridium botulinum contamination.
Skipanon Brand Seafoods LLC is recalling approximately 57,000 cans of smoked sockeye salmon due to lack of documentation and possible under-processing.
Skipanon Brand Seafoods LLC is recalling approximately 57,000 cans of smoked Chinook salmon due to lack of documentation and possible under-processing, which could lead to Clostridium botulinum contamination.
Skipanon Brand Seafoods LLC is recalling all canned and pouch seafood products due to lack of documentation and possible under-processing, which could lead to Clostridium botulinum contamination.
Skip Hop is recalling Moonlight & Melodies projection crib mobiles because the strap attaching the product to the crib rail can break, posing an injury hazard if the product falls on an infant.
Implant Direct Sybron Manufacturing is recalling 26 lots of DirectGuide Drill Extenders because the drill may drop during use.
Skipanon Brand Seafoods LLC is recalling approximately 57,000 cans of smoked sturgeon due to lack of documentation and possible under-processing, which could lead to Clostridium botulinum contamination.
LeMaitre Vascular is recalling Over-the-Wire Embolectomy Catheters due to a manufacturing issue that may compromise sterility.
Aston Martin is recalling specific 2010-2016 models because interior door unlocking mechanisms may fail when locked from outside, potentially trapping occupants.
Sterilmed is voluntarily recalling reprocessed tourniquet cuffs because the company cannot assure the sterility of all units in the affected lots.
GE Medical Systems is recalling 125 Revolution CT scanners worldwide due to potential image artifacts in head scans that may mimic pathology. No injuries have been reported.
LeMaitre Vascular is recalling 4,315 Over-the-Wire Embolectomy Catheters due to a manufacturing issue that could compromise sterility.
Skipanon Brand Seafoods LLC is recalling all cans and pouches of its seafood products due to lack of documentation and possible under-processing, which could lead to Clostridium botulinum contamination.
Skipanon Brand Seafoods is recalling canned smoked peppered Chinook salmon due to lack of documentation and possible under-processing, which could allow Clostridium botulinum contamination.
LeMaitre Vascular is recalling 4,315 embolectomy catheters worldwide due to a manufacturing defect that may compromise packaging sterility.
Olympus is recalling 182 ENDOEYE HD II video telescopes because a damaged temperature sensor can cause the tip to overheat, posing a burn risk to patients and users.
RemedyRepack, Inc. is recalling 65 vials of Humulin 70/30 insulin due to incorrect storage instructions on the label.
Pfizer is recalling Norpace CR (disopyramide phosphate) capsules because they failed to meet dissolution specifications. The recall covers specific lots distributed nationwide.
LeMaitre Vascular is recalling 4,315 units of NovaSil Silicone Embolectomy Catheters due to a manufacturing issue that may compromise sterility.
RemedyRepack Inc. is recalling Ascorbic Acid 500 MG/ML Injection vials because they contain incorrect storage instructions on the label.
LeMaitre Vascular is recalling 4,315 Over-the-Wire Embolectomy Catheters due to a manufacturing issue that may compromise sterility.
BioHorizons is recalling 32 units of 5.0 x 15mm dental implants because the packaging incorrectly listed the length as 10.5mm.
LeMaitre Vascular is recalling NovaSil Embolectomy Catheters due to a manufacturing issue that could compromise packaging sterility.