State
73,584 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, 1,508 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,701 (29%) are Severe.
Which agencies issued them
These figures cover only the 12,947 recalls whose distribution notice names New York specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Steris Corporation is recalling 374 units of RAPICIDE PA Part A High-Level Disinfectant because a blocked vented cap may cause the bottle to swell and release vapor or liquid, posing an injury risk.
Houston Rx LLC is recalling 64 vials of Tirzepatide/Niacinamide injection due to a lack of assurance of sterility. The product was distributed nationwide.
Medline is recalling 56 surgical convenience kits because the cannula components may leak or break during use.
Steris is recalling 11,806 units of its RAPICIDE PA high-level disinfectant because a blocked vented cap can cause the bottle to swell and release vapor or liquid, risking user injury.
Medline Industries is recalling 36,199 surgical convenience kits nationwide because cannula components do not meet ISO 80369-7 dimensional requirements, posing a risk of leaking or breaking during use.
Becton Dickinson is recalling 669,200 units of the BD Phoenix Panel NMIC-306 due to potential quality control failures with Klebsiella pneumoniae ATCC BAA-1705.
Hyundai is recalling 2026 Venue, Elantra N, Elantra Hybrid, and Elantra vehicles because wheel lug nuts may loosen, allowing the wheel to detach.
Cadwell Industries is recalling 23 IOMAX Cortical Modules because a defective circuit board may cause unintended electrical stimulation to patients.
Audi is recalling 2024-2025 Q4 E-Tron and Q4 Sportback E-Tron vehicles because the high-voltage battery may fail and cause a fire.
Jenavalve Technology Inc. is recalling 111 units of JenaValve Trilogy Delivery Catheters due to a defect that may prevent heart valve deployment.
Instrumentation Laboratory is recalling 1,414 units of HemoslL AcuStar HIT-lgG(PF-4) in vitro diagnostic reagents due to a potential for invalid calibration curves or negative mean bias of up to 47% with patient samples.
Jenavalve Technology Inc. is recalling 108 units of the JenaValve Trilogy Delivery Catheter due to a defect that may prevent heart valve deployment.
Medtronic is recalling specific Grafton DBM and Grafton Plus DBM products because the donor tissue tested positive for Clostridium butyricum, posing a potential infection risk.
Beckman Coulter is recalling IQ200 SPRINT, SELECT, and ELITE hematology analyzers because a check valve defect may cause fluid leaks, creating slip, chemical, and biohazard risks.
Medline is recalling 193,374 surgical convenience kits nationwide because the cannula components do not meet ISO 80369-7 dimensional requirements and may leak or break during use.
Medline Industries is recalling 1,900 surgical convenience kits because cannula components do not meet ISO 80369-7 standards and may leak or break during use.
Baxter Healthcare is recalling Likorall Overhead Lifts because a motor shaft breakage combined with reduced safety system performance may cause the lift strap to lower quickly, posing a risk of patient injury.
Becton Dickinson is recalling 553,625 BD Phoenix Panel NMIC-312 units nationwide because the CPO Ambler classification feature may misclassify Klebsiella pneumoniae.
Autocar is recalling 2022-2027 Xpeditor trucks with Cummins L9 engines because fuel hoses may separate, causing leaks, engine stalls, and fire risks.
Medline Industries is recalling 8,374 surgical convenience kits nationwide because the cannula components do not meet ISO 80369-7 dimensional requirements and may leak or break during use.
Medline is recalling 6,069 surgical convenience kits because the cannula components do not meet ISO 80369-7 dimensional requirements and may leak or break during use.
Daimler Trucks North America is recalling 2027 Thomas Built Buses Saf-T-Liner C2 school buses because a heater hose may rupture, causing hot coolant to leak and burn occupants.
Stewart's Shops is recalling Vanilla Heavenly Medley ice cream because it may contain pieces of metal.
Sarnova HC is recalling 2,500 Curaplex Capnography kits because they were assembled with pediatric nasal cannulas instead of adult ones.
Medline is recalling 472 surgical convenience kits because the cannula components do not meet ISO 80369-7 requirements, which may cause leaking or breaking during use.