State
72,919 recalls have nationwide distribution and so reach Maine. 3,894 additional recalls listed Maine specifically in their distribution scope.
Of the 3,894 recalls naming Maine we have scored against our rubric, 468 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 791 (20%) are Severe.
Which agencies issued them
These figures cover only the 3,894 recalls whose distribution notice names Maine specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Samson International is recalling Universal Broadmoor Bellevue and Oaklynn canopy bed frames because the canopy beams can collapse. Four consumers sustained contusion injuries.
E Mishan & Sons is recalling Granitestone Diamond Pro Blue sauté pans because the metal cap on the handle screw can detach and forcefully eject when heated. One injury has been reported.
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.
Beestech spiral children's tower toys are being recalled because they contain small balls and are intended for children under three, violating the mandatory standard for toys.
Member's Mark Valentine children's pajama sets are being recalled because they violate the mandatory standards for flammability of children's sleepwear.
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.
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.
Keystone RV is recalling 172 Montana fifth wheel recreational trailers because the underbelly may be improperly secured and can detach.
General Motors is recalling 32,988 Chevrolet Corvette vehicles because a software error may prevent detection of a rear turn signal light failure.
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.
General Motors is recalling 276,879 Chevrolet Malibu vehicles because the rearview camera screen may display a distorted or blank image.
Gavoyeat Halloween Light-Up Rings party favors are being recalled because the battery compartment contains button cell batteries that can be easily accessed by children.
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.
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.
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.
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 20402-401 because the probes may rupture or burst during activation. The FDA has classified this recall as Class I.
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 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 ProGuide Chronic Dialysis Catheters because a design defect in the 16F dual-valved splittable sheath introducer may prevent it splitting as intended.
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.
Isuzu is recalling 2025-2027 commercial trucks because wire harnesses may chafe, causing engine stalls, brake failures, or fires.
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.