State
72,992 recalls have nationwide distribution and so reach Indiana. 9,556 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,556 recalls naming Indiana we have scored against our rubric, 1,903 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,136 (22%) are Severe.
Which agencies issued them
These figures cover only the 9,556 recalls whose distribution notice names Indiana specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
West-Ward Columbus is recalling Methadone Hydrochloride Tablets, 5mg, in unit-dose packaging due to illegible product identification on individual tablets. Lot AC2556A was distributed nationwide.
GKN Automotive is recalling replacement driveshafts for specific BMW Mini and Land Rover models because they can crack or break, increasing the risk of a crash.
Palfinger is recalling 2017-2025 GLS 55 and FHS 55 forklifts because rear marker lights are installed in the wrong location, reducing visibility.
Forest River is recalling 2025 Shasta Oasis and Spirit travel trailers because a cracked burner tube may cause a gas leak and fire risk.
N&B Mobility Solutions is recalling Nivion NSP01 charger adapters due to electrical arcing and shock risks. Owners should contact Nivion for a free replacement.
Winnebago is recalling certain 2025 Minnie Winnie and Spirit motorhomes because the spare tire carrier mounting bolts may loosen, allowing the carrier to detach.
Kia is recalling certain 2024-2025 Sorento vehicles because a Body Domain Control Unit software error may cause a loss of low beam headlights and taillights.
Bestway Sandwiches Inc. is recalling frozen chicken and cheese taquitos due to possible metal contamination. One consumer reported a dental injury.
GNMart LLC is recalling FORCE FOREVER 400mg tablets nationwide after the FDA found the product contains undisclosed Diclofenac and Dexamethasone. The Class I recall affects all lots of this dietary supplement product.
Reser's Fine Foods is recalling its Gyro Kit With Trays due to Salmonella contamination in the tzatziki sauce. 705 cases were distributed to food service establishments across 19 states.
Grimmway Farms is recalling approximately 4,057 cases of organic whole carrots distributed nationally due to potential E. coli O121:H19 contamination. No illnesses have been reported.
Grimmway Enterprises is recalling organic whole and juice carrots sold under multiple brands due to potential contamination with E. coli O121:H19. The recall affects carrots distributed across the U.S., territories, and certain foreign countries.
Grimmway Farms is recalling organic baby carrots sold under multiple brands due to potential E. coli O121:H19 contamination affecting approximately 218,705 cases distributed nationwide and internationally.
Grimmway Farms is recalling organic baby carrots (Cal-Organic and Marketside brands) due to potential E. coli O121:H19 contamination affecting 10,482 cases distributed across the U.S., Puerto Rico, and internationally.
Grimmway Farms is recalling approximately 21,094 cases of Organic Baby Carrots that may be contaminated with E. coli O121:H19. The product was distributed across 38 U.S. states, Puerto Rico, and Canada, UAE, Hong Kong, and Colombia.
Reser's Fine Foods is recalling FCF Item 404885 Gyro Kit No Trays due to potential Salmonella contamination from implicated cucumber in the tzatziki sauce cups. The product was distributed to consignees in 19 states.
Medline custom nasal pack procedure kits contain non-sterile surgical components with potential endotoxin contamination. Customers should discontinue use and contact Medline.
Baxter is recalling SIGMA Spectrum Infusion Pump (Version 6) units that were released after repair without complete flow testing. The incomplete testing poses a risk of improper device operation.
Baxter Healthcare is recalling certain infusion pumps that were released after repair without complete testing. Incomplete testing could affect how the device delivers medication to patients.
Medline is recalling custom surgical procedure kits that contain non-sterile surgical supplies with potential for endotoxin contamination. The kits were distributed worldwide, including the United States, United Arab Emirates, and Canada.
See DocMan surgical convenience kits are recalled for containing non-sterile Codman Surgical Patties and Strips with potential endotoxin contamination. Kits were distributed in the US, UAE, and Canada.
Medtronic has recalled 3,981 SynchroMed implantable pumps worldwide due to software issues in application version 2.x used to program the devices.
USDA FSIS issued a public health alert for Chicken Curry Empanadas that may contain undeclared milk. Consumers with milk allergies should not consume these products.
Viona Pharmaceuticals is recalling Dapsone Gel 7.5% (2760 packs) distributed nationwide due to crystallization in the formulation. The voluntary recall affects lots T400514 and T400808.
Medline is recalling three custom surgical procedure kits due to non-sterile Codman Surgical Patties and Strips that pose a potential endotoxin contamination risk. The affected kits were distributed in the US, Canada, and the UAE.