State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
New Flyer is recalling 2,357 transit buses from 2005-2007 because front axle beams may crack and fail, risking loss of vehicle control.
Palmer and Company is recalling Palmer's Candies Cookies & Cream Bark because an ingredient may be contaminated with Salmonella.
Apotex Inc. is recalling 19,584 bottles of Cyclosporine Capsules, USP, 100 mg, because the product failed impurity specifications.
The FDA recalled Palmer's Candies Game Day Party Bowl because its ingredients may contain Salmonella bacteria.
Philips Lighting is expanding a recall of about 256,000 Metal Halide Lamps because the outer bulbs can shatter, posing fire and laceration risks.
REV Ambulance Group is recalling 69 specific 2017 Type I ambulances because overtightened rear brake bolts may cause loss of braking power.
Palmer and Company is recalling Palmer's Candies Creme De Menthe Bark because an ingredient may be contaminated with Salmonella.
Palmer and Company is recalling Peppermint Bark candy because an ingredient may be contaminated with Salmonella. The product was distributed to grocery stores in 34 states.
Palmer Candy Co is recalling Trail's End Gourmet Chocolatey Crunch because an ingredient may be contaminated with Salmonella.
Palmer's Candies is recalling Chocolatey Football Pretzels because an ingredient may be contaminated with Salmonella.
Palmer and Company is recalling 198 cases of Palmer's Candies Chocolatey Pretzels because an ingredient may be contaminated with Salmonella.
Hospira is recalling 578,784 bags of Metronidazole Injection due to a customer report of a leaking bag, which compromises sterility assurance.
Golden Flake is recalling Hot Thin & Crispy Potato Chips due to undeclared milk, a major allergen. The recall covers 14 states.
Tosoh Bioscience is recalling 682 HLC-723G8 analyzers because they may report inaccurate HbA1c values for patients with specific hemoglobin variants.
Pier 1 Imports is recalling about 363,000 glass knobs sold in the U.S. because they can break and cause lacerations.
Arrow International Inc is recalling 215,703 vascular catheter introduction kits nationwide because complaints were received regarding peel away sheaths flaring.
Falafel King is recalling 1,380 containers of Tzatziki Sauce due to undeclared milk on the label. The product was distributed in Colorado, New Mexico, Utah, and Nebraska.
Volvo is recalling 2017 S60, V60, and XC60 vehicles because side air bag inflators may fail to ignite, preventing deployment in a crash.
Forest River is recalling 2017 Rockwood and Flagstaff recreational trailers because a slide room bracket may damage the front tire, causing deflation and increasing crash risk.
Hostess Brands is recalling Holiday White Peppermint Twinkies because an ingredient may be contaminated with Salmonella. The product was distributed nationwide.
Tosoh Smd Inc is recalling 34 units of Reporting Software for the G8 analyzer because power outages cause the software to shut down.
Sandoz Inc. is recalling Transderm Scop patches because the outer carton contains incorrect instructions for cutting the patch.
Vascular Solutions is recalling 633 units of GrebSet Micro-Introducer Kits because the guidewires have a shorter shelf life than the kit expiration date.
Cardiovascular Systems Inc is recalling 8 units of the Diamondback 360 Peripheral 1.50 Classic system because a 1.50mm Solid Crown OAD was mislabeled as a 1.50mm Crown OED.
Reckitt Benckiser LLC is recalling Durex Pleasure Pack condoms because the package labeling is missing information about the active ingredient Benzocaine.