State
72,919 recalls have nationwide distribution and so reach Indiana. 9,555 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,555 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 9,555 recalls whose distribution notice names Indiana specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Tuymec Minoxidil Hair Growth Kits are being recalled because the packaging is not child-resistant, as required for minoxidil under the Poison Prevention Packaging Act.
OCUN NA is recalling Ocun Condor HMS Triple Locking Carabiners because the gate can malfunction and fail to close automatically, having to be closed by hand.
ELENKER-branded adult portable bed rails in three sizes are being recalled because users can become entrapped within the rail or between the rail and the mattress.
TecFlox hair and beard growth serum bottles are being recalled because they are not child-resistant, as required for minoxidil under the Poison Prevention Packaging Act.
General Motors is recalling 276,879 Chevrolet Malibu vehicles because the rearview camera screen may display a distorted or blank image.
BMW of North America is recalling 9,160 K 1600 motorcycles because a deteriorating seal can let moisture into the reverse gear control unit, causing it to overheat.
Sangohe adult portable bed rails models 504E and 504Q are being recalled because users can become entrapped within the rail or between the rail and the mattress.
Coluans Christmas Light-Up Rings party favors are being recalled because the battery compartment contains button cell batteries that can be easily accessed by children.
General Motors is recalling 32,988 Chevrolet Corvette vehicles because a software error may prevent detection of a rear turn signal light failure.
Keystone RV is recalling 172 Montana fifth wheel recreational trailers because the underbelly may be improperly secured and can detach.
Ajinomoto Foods North America is recalling Teppanyaki Style Vegetable Fried Rice due to the presence of glass fragments ranging from 1–3 cm long. Consumers should not eat affected products and should discard or return them.
Philips Respironics is recalling the Trilogy EV300 ventilator because using non-pneumatic nebulizers may cause a discrepancy between the set tidal volume and the volume the patient receives.
Philips Respironics is recalling the Trilogy Evo ventilator because using non-pneumatic nebulizers may cause a discrepancy between the set tidal volume and the volume the patient receives.
Merit Medical is recalling DuraMax Chronic Hemodialysis Catheters because a design defect in the 16F dual-valved splittable sheath introducer may prevent it splitting as intended.
Philips Respironics is recalling the Trilogy Evo Universal ventilator because using non-pneumatic nebulizers may cause a discrepancy between the set tidal volume and the volume the patient receives.
Erbe USA is recalling the Flexible Cryoprobe REF 20402-411 because the probes may rupture or burst during activation. The FDA has classified this recall as Class I.
Ajinomoto Foods North America Inc. is recalling Trader Joe's Japanese Style Fried Rice with Edamame, Tofu, and Hijiki Seaweed (1 lb. bags) due to glass fragments 1–3 cm long and 2–4 mm wide found in the product.
Erbe USA is recalling the Flexible Cryoprobe REF 20402-410 because the probes may rupture or burst during activation. The FDA has classified this recall as Class I.
Merit Medical is recalling CentrosFLO Hemodialysis Catheters because a design defect in the 16F dual-valved splittable sheath introducer may prevent it splitting as intended.
Philips Respironics is recalling the Trilogy Evo O2 ventilator because using non-pneumatic nebulizers may cause a discrepancy between the set tidal volume and the volume the patient receives.
Merit Medical is recalling the 16F Dual Valved Splittable Sheath Introducer in bulk non-sterile form because a design defect may prevent it splitting as intended.
Merit Medical is recalling BioFlo DuraMax Catheters because a design defect in the 16F dual-valved splittable sheath introducer may prevent it splitting as intended.
Navajo Manufacturing is recalling the Handy Solutions Neck & Shoulders Heating Pad because folding it during use raises power density in the folded area, causing excessive temperatures the limit device cannot sense.
Isuzu is recalling 2025-2027 commercial trucks because wire harnesses may chafe, causing engine stalls, brake failures, or fires.
Merit Medical is recalling ProGuide Chronic Dialysis Catheters because a design defect in the 16F dual-valved splittable sheath introducer may prevent it splitting as intended.