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.
QualiTech is recalling 40,080 lbs of dry blueberry and strawberry blend due to potential E. coli O121 contamination.
Forest River is recalling 2016 Rockport cargo and work trucks because the rear ramp may damage fuel connections, causing engine stalls and crash risk.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because splits or holes may compromise sterility in custom surgical kits.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because they may contain splits or holes that compromise sterility.
Vascular Solutions is recalling Twin-Pass dual access catheters because excess manufacturing material may remain at the tip or in the distal lumen.
Arbor Pharmaceuticals is recalling Cetylev (acetylcysteine) effervescent tablets because incomplete seals on the blister packaging allow moisture to enter, causing the tablets to swell.
Ford is recalling specific 2010-2012 Escape and 2010-2011 Mariner vehicles because a cracked fuel delivery module may cause a fuel leak, increasing the risk of fire.
Del Monte is recalling cut green beans and field peas with snaps due to a customer complaint of finding crawfish parts in the product.
QualiTech is recalling 176,900 lbs of PE Blueberries due to potential E. coli O121 contamination. The product was distributed to multiple US states and Canada.
Heartware, Inc. is recalling Ventricular Assist System Controllers due to loose connector ports. The recall affects 4,235 units worldwide, including 7,272 in the U.S.
Del Monte is recalling approximately 15,000 cases of canned field peas and green beans after a customer complaint reported finding crawfish parts in the product.
Vascular Solutions is recalling Twin-Pass dual access catheters because excess manufacturing material may remain at the catheter tip or within the distal rapid exchange lumen.
Ford is recalling 2017 F-250 through F-550 Super Duty trucks because a fuel shield may detach, causing a leak that increases fire risk.
Teleflex Medical is recalling Willy Rusch Tracheostomy Tube Sets because the connector may disconnect from the tube during use.
QualiTech, Inc. is recalling 1,400 lbs of FE Rainbow Blend because a supplier notified the company of potential E. coli O121 bacteria in the material.
Windstone Medical Packaging is recalling 304 Endoscopy Packs because disposable gloves in the kits may have splits or holes that compromise sterility.
RTI Surgical is voluntarily recalling 66 units of Streamline OCT spinal rods due to potential cracks that could reduce strength and cause patient injury.
QualiTech is recalling 400 lbs of FE Bacon 286 because a supplier reported the potential presence of E. coli O121 bacteria.
Awareness Corporation is recalling 2,697 bottles of Boost Tea dietary supplement due to potential Salmonella contamination. The product was distributed in 34 U.S. states and D.C.
Windstone Medical Packaging is recalling 816 Extremity Tray kits because the included Medtronic gloves may have splits or holes that compromise sterility.
X Spine Systems is recalling 1,186 Calix T PEEK Lumbar System trial devices because components may detach and lodge in the intervertebral space during surgery.
QualiTech is recalling 4,150 lbs of red bell peppers due to potential E. coli O121 contamination. The product was distributed in ten US states and Canada.
QualiTech, Inc. is recalling 300 lbs of green bell peppers due to potential E. coli O121 contamination. The product was distributed to multiple US states and Canada.
Windstone Medical Packaging is recalling 12 Major Laparotomy Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.
X Spine Systems is recalling 195 units of Calix T PEEK Lumbar System TLIF Rasps because the tools may detach and become lodged in the surgical site.