State
73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Gertrude Hawk Chocolates is recalling R.H. Macy & Co. Milk Chocolate Covered Peanut Butter Pretzels because the packaging failed to list almonds and pecans.
GE Healthcare is recalling 119 Vscan Extend ultrasound devices because the LVivo EF app may overestimate ejection fraction values, potentially affecting clinical assessments.
Gertrude Hawk Brands is recalling R.H. Macy & Co. Dark Chocolate Sea Salt Caramels because the packaging failed to disclose the presence of almonds and pecans.
Patriot Pyrotechnics is recalling 22 types of fireworks because they are overloaded with pyrotechnics, creating explosion and burn risks. No injuries have been reported.
Arrow International Inc is recalling Arrowg+ard Blue Advance JACC products due to an incorrect expiration date listed by Lidstock.
Arrow International Inc. is recalling 105 units of Arrow PICC Kits due to incorrect expiration dates on the packaging.
Zimmer Biomet is recalling 313 Mobi-C 14mm Distraction Screws because they were incorrectly labeled as 12mm length screws.
Arrow International Inc is recalling 20 units of Arrow PICC with Chlorag+ard Technology due to an incorrect expiration date on the label.
Arrow International Inc is recalling 983 units of Arrow PICC with Chloraguard Technology due to incorrect expiration dates.
Zydus Pharmaceuticals USA Inc. is recalling Pramipexole Dihydrochloride Tablets 0.5 mg due to cross-contamination caused by a cleaning failure.
Stryker GmbH is recalling 1,600 Endotrac EPF/EGR Hook/Triangle Blade Kits because the sterile bag seal integrity may be compromised.
Arrow International Inc is recalling 48 units of Arrowg+ard Blue Advance PICC catheters because the product has an incorrect expiration date.
Arrow International Inc. is recalling Arrow JACC devices with Chloraguard Technology due to an incorrect expiration date on the packaging.
Arrow International Inc. is recalling 66 units of Arrow PICC powered by Arrow VPS Stylet because the product has an incorrect expiration date.
Sun Pharmaceutical is recalling Wal-Fex D allergy and congestion tablets because testing showed impurity levels above or near specification limits.
Arrow International Inc is recalling 108 units of Arrow PICC with Chloraguard Technology because the product was labeled with an incorrect expiration date.
Zydus Pharmaceuticals is recalling Pramipexole Dihydrochloride Tablets 0.25 mg due to cross-contamination caused by cleaning failures.
Arrow International Inc is recalling 1,840 units of Arrow PICC Kits because the product labels display an incorrect expiration date.
CooperSurgical is recalling 19 LEEP Precision Integrated Systems because incorrect fuses may have been installed in the generator.
Arrow International Inc. is recalling 9 units of Arrow JACC with Chloraguard Technology due to incorrect expiration dates on the product.
Zydus Pharmaceuticals USA Inc is recalling Pramipexole Dihydrochloride Tablets 0.25 mg due to cross contamination caused by a cleaning failure.
Arrow International is recalling 350 units of Arrowg+ard Blue Advance PICC catheters because the product labels display an incorrect expiration date.
Arrow International Inc is recalling 279 units of Arrowg+ard Blue Advance PICC catheters because the products display an incorrect expiration date.
Arrow International Inc is recalling 2 units of Arrow JACC with Chloraguard Technology due to an incorrect expiration date on the product label.
Sun Pharmaceutical is recalling Allergy Relief D tablets because testing showed impurities above or near specification limits.