State
72,971 recalls have nationwide distribution and so reach New York. 12,905 additional recalls listed New York specifically in their distribution scope.
Of the 12,905 recalls naming New York we have scored against our rubric, 1,501 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,135 (24%) are Severe.
Which agencies issued them
These figures cover only the 12,905 recalls whose distribution notice names New York specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
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.
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.
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.
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.
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.
Seal the Seasons Frozen Organic Blueberries are being recalled after the firm was notified by its supplier that the product is contaminated with Listeria monocytogenes. 208 cases 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.
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.
Baxter SIGMA Spectrum Infusion Pump V6 units are being recalled because certain pumps may have an incorrect version of software. 14 units 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.
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.
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.
Cotton Candy Twirl Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.
Lisinopril and Hydrochlorothiazide Tablets 20 mg/12.5 mg are being recalled after a complaint that a sealed bottle contained a foreign tablet identified as atazanavir and ritonavir. 58,968 bottles 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.
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.
Chocolate Crunch Cake Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.
BLS laser light show projectors, models CLUB 1000, 2000 and 4000, are being recalled because the remote interlock connector required by federal regulation was not installed or was not wired. 12 units affected.
EMPOWR 3D Knee Tibial Insert E-PLUS units are being recalled because of a packaging discrepancy in which incorrect tibial inserts were packaged. 20 units are affected.
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.
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.
Rizatriptan Benzoate Tablets USP 5 mg are being recalled after detection of N-nitroso-dimethyl-rizatriptan above the FDA recommended acceptable intake limit.
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.
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.