State
73,100 recalls have nationwide distribution and so reach Indiana. 9,585 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,585 recalls naming Indiana we have scored against our rubric, 1,913 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,148 (22%) are Severe.
Which agencies issued them
These figures cover only the 9,585 recalls whose distribution notice names Indiana specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Kido Sports is recalling Scorpion EXO Covert X and Harley-Davidson HD-X07 helmets because they may not stay securely fastened, increasing injury risk.
Volkswagen is recalling certain 2022-2024 Golf R and Golf GTI, and 2024 Atlas and Atlas Cross Sport vehicles because the rearview camera image may be delayed or deactivated after shifting into reverse.
REI is recalling Co-op Cycles REV children's bicycles (12-, 16-, and 20-inch models, 2022-2024) because the training wheel assembly knob can loosen and detach, creating fall and injury hazards.
Toyota is recalling certain 2024 Lexus RX and 2024-2025 NX vehicles because driver and front passenger head restraints may be removed inadvertently without pressing the lock release, failing FMVSS 202.
GM is recalling certain 2020-2022 Bolt EV and 2022 Bolt EUV vehicles previously remedied under 21V-650, because diagnostic software may have been installed incorrectly and fail to detect defective battery modules.
Micro Bird is recalling 22,582 school buses because the rear emergency door handle may break, potentially delaying emergency access.
Daikin Comfort Technologies is recalling about 56,000 Daikin FIT, Amana Brand S-series, and Goodman SD heat pumps due to a power interruption defect that can cause the units to provide heat even when the thermostat is set to cooling mode, posing a risk of excessive heat exposure.
Nissan is recalling 2024 Frontier vehicles because an oversized ball joint may separate, causing loss of steering control and increasing crash risk.
ZOLL is recalling operator's guides for the ZOLL 731 Ventilator because they omit critical MRI safety information. Missing distance guidance could cause the ventilator to malfunction during MRI procedures.
Hamilton Medical AG is recalling the HAMILTON-C6 ventilator due to a sensor failure that may prevent re-initiation after reconnection, potentially causing hypoxia.
Howmedica is recalling the Gray Revision Instrument System Accessory Tray/Case due to a design flaw that may enable reuse and re-sterilization of single-use, sterile-packaged instruments.
Howmedica Osteonics Corp. is recalling HRIS Storage & Sterilization Cases (Part 6210-9-900) due to a design flaw that may allow reuse and resterilization of single-use, sterile instruments. This poses a contamination and infection risk.
Daimler Trucks North America is recalling 162 Thomas Built Buses Saf-T-Liner C2 and C2 Jouley school buses because the emergency exit alarm may not sound.
OSSOS-SANS Reforzado tablets are being recalled because they contain undeclared active pharmaceutical ingredients—diclofenac and methocarbamol—and were marketed without FDA approval.
Beaver Visitec International is recalling 126 Xstar Safety Slit Knives with incorrect blade configuration. The recalled knives have the bevel oriented to the back instead of the front.
Ethicon is recalling VICRYL Plus Antibacterial Sutures due to a packaging machine defect that created holes in the primary packaging, potentially compromising product sterility. Affected sutures may pose an infection risk.
Polestar is recalling certain 2021-2024 Polestar 2 vehicles because Infotainment Head Unit software may prevent the rearview camera image from displaying, failing FMVSS 111.
C.R. Bard Inc is recalling 6,420 Foley catheter trays nationwide because some devices may not display temperature readings or may display erratic readings. The malfunction could affect patient monitoring.
Ethicon is recalling 56,952 units of PDS II polydioxanone sutures distributed worldwide because a packaging defect resulted in compromised sterility, which could lead to infection. No illnesses have been reported.
Breckenridge Pharmaceutical recalls Duloxetine 60mg capsules nationwide due to N-nitroso-duloxetine impurity levels exceeding FDA interim limits. Affected lots had current good manufacturing practice (CGMP) deviations.
Eugia US LLC recalls 70,125 vials of Dexamethasone Sodium Phosphate injection due to failed impurity specifications. Testing found sulfonic acid adduct of dexamethasone phosphate exceeded allowed limits.
Teva Pharmaceuticals is recalling 34,448 bottles of Amoxicillin and Clavulanate Potassium Tablets USP (Chewable 400mg/57mg) distributed nationwide due to subpotency. The recall is voluntary and initiated by the firm.
Baxter Healthcare is recalling Centrella Max and Pro+ hospital bed mattresses that may develop delaminated top covers when cleaned with bleach-containing solutions. The mattresses prevent and treat pressure injuries.
NxStage PureFlow-B hemodialysis solution bags may burst during preparation, releasing caustic electrolyte fluid that can cause chemical burns. Affected units are distributed nationwide.
Ethicon recalls PDS Plus Antibacterial sutures due to packaging defects that compromised sterility. The affected units may cause infection if used in surgery.