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.
Polymedco is recalling Sediplast tubes because pressure buildup may eject the cap, releasing blood and creating a biological hazard for operators.
Carolina Infusion, LLC is recalling Tri-MIX injectable syringes due to a lack of assurance of sterility related to processing equipment.
Stryker is recalling Bard EP XT Decapolar Steerable Diagnostic EP Catheters due to a potential sterile barrier breach that could lead to particulate embolization, infection, or thrombus formation.
A&P CREATIONS is recalling biQ-FEL beverage bottles containing undeclared Sildenafil and Tadalafil. The product was distributed nationwide.
Carolina Infusion, LLC is recalling Tri-MIX injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.
Carolina Infusion LLC is recalling QUAD-MIX injectable compounded product nationwide due to sterility concerns.
Philips Medical Systems is recalling 539 Spectral CT systems due to software issues that may cause image artifacts, wrong slice thickness, or unintended system motion.
J K Patisserie & Bakery LLC is recalling croissants because egg was not declared in the Contains statement. The product was distributed in New York and New Jersey.
J K Patisserie & Bakery LLC is recalling 87 units of Lemon Blueberry Loaf because the product contains undeclared soybean oil and soy lecithin.
PACCAR is recalling 310 model-year 2027 Kenworth and Peterbilt trucks because improperly secured sleeper bunk webbing may fail to restrain occupants during a crash.
J K Patisserie & Bakery LLC is recalling 610 units of chocolate chip cookies sold in New York and New Jersey because soy was not declared in the Contains statement.
Steris Corporation is recalling VERIFY Dual Species Self-Contained Biological Indicators because the spore population may fall below specifications, potentially leading to false sterilization results.
Beak & Skiff Sanitizer Alcohol Antiseptic 80% is being recalled because FDA analysis found acetaldehyde above specification limits in the product. The recall affects bottles distributed in New York and through online sales.
Avid Medical, Inc. is recalling 30 DAVINCI LAP/GYN kits (Model WRNM037-16) because they may be contaminated with a lubricant used during manufacturing.
Onkos Surgical is recalling My3D Personalized Pelvic Implants that were inadvertently mixed up and distributed to incorrect customers.
AVID Medical, Inc. is recalling 33 Endovascular Packs (Model VAPX014-04) because they may be contaminated with a lubricant used during manufacturing.
AVID Medical, Inc. is recalling 20 Urology Major kits (Model WRNM058-10) because they may be contaminated with a lubricant used during manufacturing.
DRG International is recalling Sperm Ab ELISA kits due to a potential for false negative patient results. The recall covers 211 units distributed in the US and several international countries.
Preferred Pharmaceuticals is recalling Lidocaine Ointment USP, 5% due to failed content uniformity specifications. The product is distributed nationwide.
AVID Medical, Inc. is recalling 96 Heart Prep Trays (Model MECV97W) because they may be contaminated with a lubricant used during manufacturing.
Onkos Surgical is recalling My3D Personalized Pelvic Implants that were inadvertently mixed up and distributed to incorrect customers.
Cipla USA, Inc. is recalling specific lots of Fosfomycin Tromethamine granules because they failed impurity and degradation specifications.
GRI Medical is recalling Halyard Laparoscopy Comprehensive Pack II kits because they contain a latex urethral catheter despite being labeled as latex-free.
AVID Medical, Inc. is recalling 28 units of EURO053 plastic trays potentially contaminated with manufacturing lubricant. The units were distributed in AZ, CA, FL, MD, NE, and TX.
Beckman Coulter is recalling DxC 500i Clinical Analyzer Modules because a software issue can cause test units to revert to defaults without warning, potentially resulting in falsely elevated reported results.