State
73,718 recalls have nationwide distribution and so reach Indiana. 9,596 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,596 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 2,534 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,596 recalls whose distribution notice names Indiana specifically. The 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ameditech is recalling 41,340 units of First Check 2 Panel Drug Cups because the products failed to consistently detect compounds at labeled levels.
Strides Inc. is recalling 11,280 bottles of Potassium Chloride Extended-Release Tablets because they failed to meet dissolution specifications.
pH-D Feminine Health is recalling Boric Acid Vaginal Suppositories because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Ameditech Inc is recalling Alere iCup Drug Detection cups because immunoassay enzymes failed performance tests, preventing consistent detection of compounds.
Ameditech is recalling Fastect II Drug Screen Dipstick Tests because they failed to consistently detect compounds at labeled levels.
Ameditech Inc is recalling TDDA Drugs of Abuse Cups because the immunoassay enzymes failed to consistently detect all compounds at labeled levels.
Beckman Coulter is recalling 219 units of UIBC reagent lot 2690 because it produces erroneously high patient results at the low end of the linear range.
Ameditech is recalling iCup Dx14 Drug Screen Cups because immunoassay enzymes failed performance tests, causing inconsistent detection of compounds.
Ameditech is recalling 47,005 units of First Check 14 Panel Drug Cups because immunoassay enzymes failed performance tests, preventing consistent detection of compounds.
Arbor Pharmaceuticals is voluntarily recalling Nymalize (nimodipine) oral solution because the drug is subpotent. The FDA classifies this as a Class III recall.
Ferrari is recalling 2018-2020 812 Superfast vehicles because the rear window may have been bonded incorrectly, potentially leading to detachment and increased crash risk.
REV is recalling certain 2020-2021 Fleetwood and Holiday Rambler motorhomes with Dometic propane stoves due to potential gas leaks that could increase fire risk. Owners should contact REV for free repair at 1-800-509-3417.
TriMark is recalling 50-200 door latches used in emergency vehicles because trip levers may fail, preventing doors from opening.
Lippert Components is recalling electric motors in Power Bedlift systems because internal gear failure may cause the bed to extend unexpectedly, increasing injury risk.
Piaggio is recalling 2020-2021 Vespa GTS 300 and GTV 300 scooters because improperly galvanized brake pipe terminals can reduce braking efficiency and increase crash risk.
REV Ambulance Group is recalling 2019 Road Rescue Type I ambulances because incorrect material in door latches may prevent doors from opening, creating a lock-in risk.
Yamaha is recalling specific 2015-2020 motorcycles and scooters because condensation on the rear reflector lens may reduce its effectiveness, increasing crash risk.
Volvo Trucks North America is recalling 2020 VNL vehicles because window hinges may fail if sleeper windows are open, posing a crash risk.
Mercedes-Benz is recalling 2020 GLC 350e hybrid vehicles because a high-voltage wiring harness shield may fail, causing an electrical malfunction and vehicle stall.
Micro Bird is recalling 75 model-year 2019 MB II buses because a grounding wire issue may cause a short circuit, increasing the risk of fire.
Keystone RV Company is recalling 2020 Hideout 290LHS recreational trailers because they were built with incorrect axles and tires, increasing the risk of a crash.
Dick's Sporting Goods is recalling Field & Stream Kayak Cradles because kayaks may fall off while driving, increasing crash risk.
The P2K Bunk Bed System motor in certain 2021 Coachmen Sportscoach and Forest River Georgetown motorhomes may fail, causing the bunk to fall while the vehicle is in motion. This increases the risk of injury or a crash.
Mercedes-Benz is recalling 2019 C 300 vehicles because the center console lock may not function properly, increasing injury risk in rear-end crashes.
Aston Martin is recalling specific 2017-2020 models because front seat air bag fasteners may not be tightened correctly, increasing injury risk.