State
72,971 recalls have nationwide distribution and so reach Montana. 3,568 additional recalls listed Montana specifically in their distribution scope.
Of the 3,568 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 3,568 recalls whose distribution notice names Montana specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Creekwood Naturals Gum Spirits of Turpentine bottles are being recalled because they violate the mandatory standard for child-resistant packaging. About 9,000 units are affected.
LIVACTI retractable mesh safety gates, model LT-BG01-3, are being recalled because a child's torso can fit through the opening between the gate and the floor. About 1,400 units are affected.
LED gloves, model ST01, are being recalled because the coin battery compartment can be easily opened by children and the spare batteries are not in child-resistant packaging. About 9,900 units affected.
Ferrari is recalling certain 2023-2025 Purosangue vehicles because the fuse box power supply and passenger-side footrest may contact each other, causing a short circuit that decreases braking ability.
BMW is recalling certain 2022-2025 i4, 2022-2024 iX, 2023-2024 i7 and 2024 i5 vehicles because electric drive motor software may shut down the high-voltage system, causing a loss of drive power.
Tiffin is recalling certain 2023-2026 motorhomes with 2.0 litre engines because the secondary alternator controller programming was not properly updated, which can stall the engine.
VITROS Chemistry Products Performance Verifier II is being recalled because quality control drift can occur with certain cholinesterase slide lots, which could produce erroneous patient results.
The NIO Intraosseous Device Adult is being recalled because a manufacturing error means the built-in stabilizer may not be released properly after deployment and insertion. 516 US units affected.
BLS laser light show projectors, models DIODE 1000, 2000 and 3000, are being recalled because the remote interlock connector required by federal regulation was not installed or was not wired. 10 units affected.
YoCrunch Low Fat Yogurt with Toppers, Vanilla with Twix bar pieces, is being recalled because of foreign material in the form of plastic pieces.
Hyundai is recalling certain 2025 IONIQ 5 vehicles because the high voltage battery may contain an improperly tightened bus bar that can short circuit. Owners are told to park outside until repaired.
Levothyroxine Sodium Tablets, USP 25 mcg in 1000-count bottles from Accord Healthcare are being recalled because the product is subpotent. 2,352 bottles are affected.
Levothyroxine Sodium Tablets, USP 100 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 9,739 bottles affected.
YoCrunch Low Fat Yogurt with Toppers, Strawberry with Granola pieces in 6 oz single serve cups, is being recalled because of foreign material in the form of plastic pieces.
SwabCap Disinfecting Caps for needlefree connectors are being recalled because an incomplete seal may let isopropyl alcohol evaporate, which may result in inadequate disinfection. 1,445,600 units affected.
Omeprazole Delayed-release Capsules USP 20 mg are being recalled because a foreign Divalproex Sodium Extended-Release 250 mg tablet was found in a bottle. 1,476 bottles affected.
The NIO-A NIO Intraosseous Device Adult is being recalled because a manufacturing error means the built-in stabilizer may not be released properly after deployment and insertion. 7,056 US units affected.
VITROS Chemistry Products Performance Verifier I is being recalled because quality control drift can occur with certain cholinesterase slide lots, which could produce erroneous patient results.
Levothyroxine Sodium Tablets, USP 50 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 54,227 bottles affected.
YoCrunch Lowfat Yogurt with Toppers, Vanilla with milk chocolate M&Ms, is being recalled because of foreign material in the form of plastic pieces.
Rizatriptan Benzoate Tablets USP 10 mg are being recalled after detection of N-nitroso-dimethyl-rizatriptan above the FDA recommended acceptable intake limit.
VITROS Chemistry Products CHE Slides supplied in Japan are being recalled because quality control drift can occur with certain Performance Verifier lots, which could produce erroneous patient results.
YoCrunch Lowfat Yogurt with Toppers two-product packages containing strawberry yogurt with M&Ms and with Oreo pieces are being recalled because of foreign material in the form of plastic pieces.
BLS laser light show projectors, models PURE 5000 and PURE 10000, are being recalled because the remote interlock connector required by federal regulation was not installed or was not wired. 3 units affected.
Levothyroxine Sodium Tablets, USP 175 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 2,344 bottles affected.