State
73,576 recalls have nationwide distribution and so reach New York. 12,947 additional recalls listed New York specifically in their distribution scope.
Of the 12,947 recalls naming New York we have scored against our rubric, 1,511 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,698 (29%) are Severe.
Which agencies issued them
These figures cover only the 12,947 recalls whose distribution notice names New York specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Steamable by Lidl Chopped Spinach is recalled due to possible Listeria monocytogenes contamination. Affected products were distributed to Lidl stores across eight states.
Envisiontec US Llc recalls FLEXCERA BASE dental resin (574 units manufactured April–September 2021) due to manufacturing in a non-FDA-registered facility and mislabeling of country of origin.
Pretty Thai Sweet Chili Stir Fry & Barbecue Sauce is being recalled due to potential undeclared peanuts. Consumers with peanut allergies should not consume the product.
Olympus OER-Elite Endoscope Reprocessors may have incorrectly assembled detergent and alcohol tank tubing, causing solutions to be dispensed in reversed cycles. This results in ineffective endoscope disinfection and potential patient exposure to residual detergent.
Hill-Rom is recalling 1,215 Liko M220 and M230 mobile patient lifts with missing bushings that cause wear and risk of patient falls. Units were distributed worldwide.
Bebe au Lait is recalling approximately 8,600 wooden teethers because the string connecting beads can come untied, releasing beads that pose a choking hazard to young children. The company has received six reports of detached beads, including one case where a child placed a bead in their mouth.
Keystone RV recalls 2022 Cougar trailers with incorrectly specified tires. Load Range D tires were installed instead of required Load Range E, creating overload and crash risk.
Hill-Rom is recalling 5,470 Liko M220 mobile lifts used in nursing homes due to a missing bushing that can cause wear and potentially lead to patient falls.
The wireless foot switch in Philips Veradius Unity medical systems can lose function due to a firmware issue. This could cause delays or interruption of medical procedures if alternative input methods are not used.
Comoto is recalling specific Bilt motorcycle helmets that may not adequately protect the wearer during a head impact, failing federal safety standards.
The TJX Companies is recalling about 7,900 Festive Lights Hanukkah Menorahs because the resin and MDF material can burn or catch fire when holding lit candles. Three incidents of burning or catching fire have been reported, with no injuries or property damage.
Audi is recalling 2022 RS 5 vehicles because the B-pillar tire and loading label displays an incorrect maximum weight, which may lead to vehicle overload.
ANI Pharmaceuticals is voluntarily recalling Alprazolam Tablets USP 0.5 mg in multiple package sizes nationwide due to cGMP (current Good Manufacturing Practice) deviations. The recall affects approximately 205,662 bottles distributed across the United States.
Aurobindo Pharma USA Inc. is recalling Moxifloxacin Ophthalmic Solution 0.5% due to failed impurities and degradation specifications. The recall affects 115,776 bottles distributed nationwide.
Philips is recalling Zenition 50 wireless foot switches (Model #718096) because a firmware issue can cause them to suddenly stop responding, potentially delaying medical procedures.
ANI Pharmaceuticals, Inc. has recalled Pyrazinamide Tablets USP 500 mg due to cGMP (current Good Manufacturing Practice) deviations. The recall affects approximately 5,477 bottles distributed nationwide.
ANI Pharmaceuticals has recalled Alprazolam Tablets USP 1.0 mg distributed nationwide due to current Good Manufacturing Practice (cGMP) deviations. The recall affects 173,499 bottles across multiple lot numbers.
Lannett Company is recalling Diazepam Oral Solution (Concentrate) 5 mg/mL due to out-of-specification results for related substances, indicating failed impurities and degradation testing.
Envisiontec US LLC recalled 795 units of FLEXCERA SMILE dental resins manufactured between April 2021 and September 2021 because they were produced in a non-FDA-registered facility and falsely labeled as German origin.
Sun Pharmaceutical is recalling Chlorthalidone Tablets USP 25 mg (Lot #P0602, expiration 03/2023) due to stainless steel microscopic wear particles, punch lubricant oil, and silicone particles from the dust cup found in the product.
ANI Pharmaceuticals is recalling Alprazolam Tablets USP 0.25 mg nationwide due to current Good Manufacturing Practice (cGMP) deviations. The recall affects multiple lot numbers of 100-count, 500-count, and 1000-count bottles distributed across the United States.
ANI Pharmaceuticals is recalling Alprazolam Tablets, USP 2.0 mg nationwide due to current good manufacturing practice (cGMP) deviations. The recall affects approximately 70,788 bottles distributed throughout the United States.
Teligent Pharma is recalling one lot of Erythromycin Topical Gel USP 2% because the product failed to meet specifications for unknown maximum related compounds.
NaturesPlus Advanced Therapeutics Glucosamine Chondroitin MSM Ultra Rx Joint Cream is being recalled due to microbial contamination identified as Pluralibacter gergoviae in a non-sterile product.
A KWIK-STIK quality control kit has an incorrect inner label. The product contains Campylobacter coli, but the inner label states Haemophilus influenzae.