State
72,968 recalls have nationwide distribution and so reach Vermont. 1,983 additional recalls listed Vermont specifically in their distribution scope.
Of the 1,983 recalls naming Vermont we have scored against our rubric, 199 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 409 (21%) are Severe.
Which agencies issued them
These figures cover only the 1,983 recalls whose distribution notice names Vermont specifically. The 72,968 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Minecraft Light-Up Slap Ruler Bracelets are being recalled because the battery compartment can be opened easily by children, violating the mandatory toy standard. About 75,900 units affected.
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.
Georgia Pine Gum Spirits of Turpentine in 4 oz glass bottles is being recalled because the packaging is not child-resistant as required by the Poison Prevention Packaging Act. About 20,000 units affected.
The detachable cover of the Pura 4 Smart Home Fragrance Diffuser is being recalled because its magnets can detach. Three reports of magnets detaching have been received. About 851,400 units 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.
General Motors is recalling certain 2026 Cadillac VISTIQ and 2025 Cadillac LYRIQ vehicles because bolts attaching the high-voltage battery to the floor may be missing or loose, creating a fire risk in a crash.
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.
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.
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.
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.
VITROS Chemistry Products CHE Slides are being recalled because quality control drift can occur with certain Performance Verifier lots, which could produce erroneous patient results.
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.
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.
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.
A YoCrunch Lowfat Yogurt with Toppers two-product package containing strawberry and raspberry yogurt with granola is being recalled because of foreign material in the form of plastic pieces.
Levothyroxine Sodium Tablets, USP 150 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 4,921 bottles affected.
YoCrunch Low Fat Yogurt with Toppers, Strawberry with milk chocolate M&Ms minis, is being recalled because of foreign material in the form of plastic pieces.
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.
Rizatriptan Benzoate Tablets USP 10 mg are being recalled after detection of N-nitroso-dimethyl-rizatriptan above the FDA recommended acceptable intake limit.
YoCrunch Lowfat Yogurt with Toppers, Vanilla with milk chocolate M&Ms, is being recalled because of foreign material in the form of plastic pieces.
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.
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.
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.
YoCrunch Low Fat Yogurt with Toppers, Vanilla with Snickers pieces, is being recalled because of foreign material in the form of plastic pieces.