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.
FDA is recalling Aplicare Castile Soap towelettes found in Foley trays and specimen kits due to bacterial contamination.
Nestle is recalling specific DiGiorno, Lean Cuisine, and Stouffer's products due to the potential presence of glass pieces.
FDA is recalling specific lots of Castile soap towelettes used in medical kits due to bacterial contamination.
CareFusion is recalling 170 Alaris PC Unit Infusion Pump Model 8000 devices because a power supply component may cause system error codes.
Toshiba is recalling 28 DRAD-3000E FPD Wireless Systems because they fail to complete image transmission, resulting in no radiographic image.
King Henry's, Inc. is recalling Fruit & Nut Medley because it may contain undeclared FD&C Yellow #6. The recall covers 3,242 units distributed across 25 US states and British Columbia.
Siemens Healthcare Diagnostics is recalling IMMULITE 2000 Estradiol Test kits because the drug fulvestrant (Faslodex) may cause falsely elevated estradiol results.
Zimmer Spine is issuing a correction notice for the Universal Clamp System to provide updated cleaning and disinfecting instructions.
AstraZeneca is recalling Tudorza Pressair inhalers because some units have actuation counters set to a number other than 60.
Roche is recalling 35 cobas p 512 pre-analytical systems because a sensor defect causes open sample tubes to drop and spill.
Siemens Medical Solutions USA is recalling six syngo X Workplace medical workstations because imported segmentation results appear mirrored, rendering them unusable for ablation procedures.
Siemens is recalling ADVIA Centaur Enhance Estradiol tests because the drug fulvestrant may cause falsely elevated results.
Zimmer Biomet is issuing a correction notice to provide updated cleaning and disinfecting instructions for the Instinct Java System and Universal Clamp System.
Cook Medical is voluntarily recalling specific lots of Ultraxx Nephrostomy Balloon Sets and Ascend AQ Ureteral Dilation Balloon Catheter Sets because of a labeling mix-up.
Neurotherm, Inc. is recalling 135 curved radiofrequency cannulas because straight needles were incorrectly labeled as curved.
Cook Medical is voluntarily recalling specific lots of Ascend AQ Ureteral Dilation Balloon Catheter Sets and Ultraxx Nephrostomy Balloon Sets due to a labeling error where packages may contain the wrong product.
Forest River is recalling 2015-2017 Georgetown RVs because a vented window was installed instead of a required secondary egress window, posing a risk of entrapment.
Forest River is recalling 2013-2016 Puma recreational trailers because tires may contact the wheel well on bumps, risking tire damage and loss of control.
Terex is recalling 2011-2016 aerial devices because inadequate welds at the boom tip may cause the platform to tilt unexpectedly, increasing the risk of user injury.
CPSC reannounced the recall of Fiskars 32-inch bypass lopper shears after additional injuries were reported. Consumers should stop using the product and contact Fiskars for a free replacement.
Terex is recalling 2007-2013 aerial devices because missing reinforcements may cause the pedestal to crack, increasing injury risk.
BMW is recalling 6,110 model year 2016 740Li, 750Li, and 750Lxi vehicles because the air bag control module may reset, preventing air bags from deploying in a crash.
Blue Bird is recalling 2011-2017 All American school buses because rear seat legs may detach in a crash, increasing injury risk.
Specialized is recalling Flux and Stix bicycle lights due to overheating risks. Consumers should stop using them and seek a free repair or replacement.
Volkswagen is recalling 2012-2014 Passat TDI vehicles because water can corrode electrical connectors, causing a short that may lead to a fire.