State
72,969 recalls have nationwide distribution and so reach Ohio. 11,723 additional recalls listed Ohio specifically in their distribution scope.
Of the 11,723 recalls naming Ohio we have scored against our rubric, 2,107 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,413 (21%) are Severe.
Which agencies issued them
These figures cover only the 11,723 recalls whose distribution notice names Ohio specifically. The 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Electric Bug Zapper Racket fly and mosquito swatters, model BZ-001, are being recalled because the rechargeable battery can catch fire when used for extended periods. About 29,000 units 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.
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.
Aiho five-drawer dressers, model AP23-W, are being recalled because they are unstable if not anchored to the wall and fail the mandatory standard under the STURDY Act. About 1,900 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.
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.
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.
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.
Baxter SIGMA Spectrum Infusion Pump V6 units are being recalled because certain pumps may have an incorrect version of software. 14 units are affected.
Kilwin's Family Assortment in 9 oz, 14 oz, 28 oz and 42 oz sizes is being recalled because of undeclared pecans. 130 lbs in total are affected.
Kilwin's Truffle Assortments in 9.5 oz, 8 oz and 4.75 oz sizes are being recalled because of undeclared pecans. 130 lbs in total are affected.
Kilwin's Mocha Truffles, in 2.5 lb bulk and 4.75 oz retail units, are being recalled because of undeclared pecans. 130 lbs in total are affected.
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.
Dubai emek Spread Pistachio Cacao Cream with Kadayif is being recalled after the FDA notified the firm that the product may be contaminated with Salmonella. 316 cases are affected.
The i-view video laryngoscope is being recalled because of the potential for faulty devices as a result of depleted batteries. 2,152 pieces are affected.
Baxter SIGMA Spectrum Infusion Pump V8 units are being recalled because certain pumps may have an incorrect version of software. 28 units are affected.
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.
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.
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.
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 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.
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.