State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Medline Industries is recalling 288 cases of Newborn Kits because the Povidone-Iodine prep pads contain subpotent iodine, falling below the 0.85% label claim.
Premier Pharmacy Labs is recalling 193 vials of Mitomycin 40 mg/mL due to a label error on the declared strength.
Medline Industries is recalling 40 cases of Sheath Removal Kits because the iodine concentration is below the labeled claim.
Jarrow Formulas is recalling one lot of Liquid L-Carnitine because a higher-than-normal micro result was found during testing.
Medline Industries is recalling sterile catheter insertion trays because the iodine concentration in the prep pads is below the labeled claim.
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework process caused set screws and sleeves to shift, potentially preventing proper assembly.
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing defect may prevent proper assembly of the device.
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework error may have displaced internal components, potentially preventing proper assembly.
Ascent Pharmaceuticals is recalling 45,875 bottles of Oxycodone Hydrochloride 15 mg tablets because the label is missing the required controlled substance symbol.
Fresenius Kabi USA is recalling 35,620 vials of Vecuronium bromide for Injection due to an out-of-specification result for a related compound.
Dr. Reddy's Laboratories is recalling Atorvastatin Calcium 10 mg tablets because stability testing showed out-of-specification results for total degradation impurities.
Dr. Reddy's is recalling 12,579 bottles of Atorvastatin Calcium 40 mg tablets because they failed impurity specifications during stability testing.
Dr. Reddy's Laboratories is recalling Atorvastatin Calcium 20 mg tablets because stability testing revealed out-of-specification total degradation impurities.
Guymon Extracts Inc. is recalling approximately 4,202 pounds of fully cooked pork products due to a processing deviation that may have allowed pathogen growth.
Lenovo is recalling approximately 78,000 ThinkPad X1 Carbon 5th Generation laptops in the US due to a potential fire hazard caused by an unfastened screw.
Tiffany & Co. is recalling Wheat Leaf Crystal Mugs because they can crack or break when exposed to hot liquids, posing burn and laceration hazards.
Kohler is recalling about 24,000 gasoline engines used in outdoor power equipment due to a faulty fuel cap that poses a fire hazard.
Ferrara is recalling specific fire-fighting vehicles because corroding rings may cause pressure relief valves to open, reducing water pressure and hindering fire-fighting efforts.
B & P Lamp Supply is recalling Golo brand 3-way lamp sockets because loose screws can cause arcing or overheating, posing a fire hazard.
Whammerdyne is recalling II Much VSR remote fuel tank vent systems because they may seep fuel, which can increase the risk of a fire.
Whammerdyne is recalling II Much VSR remote fuel tank vent systems because they may seep fuel, increasing the risk of fire.
Jaguar is recalling 2018 XE, XF, E-PACE, F-PACE, and F-TYPE vehicles because fuel rail end caps may leak, increasing the risk of a fire.
PACCAR is recalling 2017-2018 Kenworth and Peterbilt trucks because the transmission gear display may show incorrectly, potentially preventing the truck from moving.
Triple E is recalling 2002-2013 recreational vehicles because Kidde fire extinguishers may clog or detach, potentially failing to discharge during a fire.
Lance is recalling 2018 travel trailers because the battery may fall out of its compartment while in motion, creating a road hazard.