State
73,827 recalls have nationwide distribution and so reach Indiana. 9,598 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,598 recalls naming Indiana we have scored against our rubric, 1,908 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,536 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,598 recalls whose distribution notice names Indiana specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
QualiTech is recalling 3,200 lbs of FE Jalapeno 709 due to potential E. coli O121 contamination. The product was distributed in 10 US states and Canada.
Dollar General is recalling Soft Baked Chocolate Brownie Cookies due to the presence of mold. Consumers should discard the product or return it for a refund.
QualiTech is recalling FE Jalapeno 321A because a supplier reported the potential presence of E. coli O121 bacteria.
Windstone Medical Packaging is recalling 852 Major General Packs because Medtronic gloves inside may have splits or holes that compromise sterility.
Windstone Medical Packaging is recalling 115 Peri Kits (PSS1037) because the included Medtronic gloves may contain splits or holes that compromise sterility.
Vascular Solutions is recalling Twin-Pass RX Dual Access Catheters because excess manufacturing material may remain at the tip or within the distal lumen.
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.
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.
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.
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.