State
72,940 recalls have nationwide distribution and so reach Montana. 3,567 additional recalls listed Montana specifically in their distribution scope.
Of the 3,567 recalls naming Montana we have scored against our rubric, 689 (19%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 783 (22%) are Severe.
Which agencies issued them
These figures cover only the 3,567 recalls whose distribution notice names Montana specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
About 1,100 Wilteexs bioethanol fuel bottles are being recalled because they lack the flame mitigation devices required by the Portable Fuel Container Safety Act.
About 76,500 WLIVE fabric 12-drawer dressers are being recalled because they are unstable when not anchored to a wall; one tip-over has been reported with no injuries.
About 90,800 E-Z-GO personal transportation vehicles are being recalled because fuel can leak at the quick-connect fitting between the fuel line and the fuel injector.
About 4,300 model year 2017-2024 Yamaha DR2A and DR2E personal transportation vehicles are being recalled because they can fail to brake. No incidents have been reported.
About 19,300 model year 2021-2025 Yamaha Drive 2 personal transportation vehicles are being recalled because they lack stop lights. No incidents have been reported.
Jaguar Land Rover is recalling specific 2025-2026 models because moisture in the gear shift module may cause the gear position indicator light to fail, increasing crash risk.
About 700 AOWOS 12-drawer dressers sold on Walmart.com are being recalled because they are unstable when not anchored to a wall and violate the STURDY Act standard.
About 280 Belivium baby loungers are being recalled because low sides, an over-thick sleeping pad and oversized foot openings create an unsafe infant sleeping environment.
Western United Fish Company is recalling 3,314.7 lbs of Kirkland Signature Ahi Tuna Wasabi Poke after its green onion supplier reported a Listeria monocytogenes positive test result.
CareFusion is recalling BD Alaris Pump Infusion Sets because the pump module used with them may perform outside established ranges for flow rate, bolus accuracy and occlusion alarm timing.
GenoGenix is recalling NAD+ for Injection at 100 mg/mL and 200 mg/mL from one lot for microbial contamination of sterile products, with elevated endotoxin levels.
Abiomed is recalling 10,153 Automated Impella Controllers over potential cybersecurity vulnerabilities related to the controller's operating system.
BMW is recalling 2018 328D diesel vehicles because a leaking EGR cooler can cause smoldering particles and a melting intake manifold, increasing the risk of a fire.
International is recalling 2026 IC Bus CESB school buses because a transmission shift actuator may not be calibrated properly, preventing reverse gear engagement.
Winnebago is recalling specific travel trailers because the Federal tire label may list the incorrect tire size, creating a risk of installing the wrong tire.
GenoGenix is recalling L-Arginine for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Major Pharmaceuticals is recalling 1,256 blister packs of Chlorpromazine Hydrochloride Tablets USP 25 mg because N-Nitroso Desmethyl Chlorpromazine was present above the recommended intake limit.
Accord Healthcare is recalling 54,432 bottles of Levothyroxine Sodium Tablets USP 88 mcg after long-term stability testing found assay content below the approved specification range.
GenoGenix is recalling preserved Ascorbic Acid (Vitamin C) for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling Zinc Chloride for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling BPC-157 for Injection, 15mg/10mL vial, from a single lot for lack of assurance of sterility.
RC Outsourcing is recalling 2,669 prefilled Bevacizumab 1.75 mg/0.07 mL intravitreal syringes for lack of assurance of sterility.
Major Pharmaceuticals is recalling 2,064 fifty-tablet blister packs of Chlorpromazine Hydrochloride Tablets USP 25 mg because a nitrosamine impurity exceeded the recommended intake limit.
GenoGenix is recalling EDTA for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling combined BPC-157/Thymosin Beta-4 for Injection across three lots for lack of assurance of sterility.