State
73,817 recalls have nationwide distribution and so reach New York. 12,956 additional recalls listed New York specifically in their distribution scope.
Of the 12,956 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 3,702 (29%) are Severe.
Which agencies issued them
These figures cover only the 12,956 recalls whose distribution notice names New York specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Banner Pharmacy Services is recalling 481 bags of Norepinephrine Bitartrate in 0.9% Sodium Chloride due to a lack of assurance of sterility.
Banner Pharmacy Services is recalling Oxytocin 30 units in 0.9% Sodium Chloride bags because the FDA determined there is a lack of assurance of sterility.
Heartland is recalling 2018 Prowler and Trail Runner trailers because electric brake wires may be severed by spring hangers, increasing crash risk.
Banner Pharmacy Services is recalling fentanyl citrate syringes because the agency could not ensure the product was sterile.
Pharmedium Services, LLC is voluntarily recalling Oxytocin 20 units in Lactated Ringer's Injection USP bags because the drug was found to be subpotent.
Pharmedium Services, LLC is voluntarily recalling 2,232 bags of compounded Oxytocin injection because the drug was found to be subpotent.
Pharmedium Services, LLC is voluntarily recalling 1,152 bags of compounded Oxytocin 40 units in Lactated Ringer's USP because the drug was subpotent.
Nissan is recalling 2017-2018 Infiniti QX30 vehicles because the driver's air bag may deploy unexpectedly due to steering component grounding issues.
FDA requested the removal of specific energy treatment settings from 12 Ablatherm ultrasound systems in the U.S. pending clinical data evaluation.
Pharmedium Services, LLC is voluntarily recalling 390 bags of compounded Oxytocin 20 units in Lactated Ringer's Injection due to subpotent drug levels.
Little Mass is recalling about 2,300 children's nightgowns and pajama sets because they fail to meet federal flammability standards, posing a risk of burn injuries.
Heartland is recalling 2018 Pioneer recreational trailers because the propane manifold block may be mounted too close to the shackle, creating a leak risk.
Nucletron BV is recalling Oncentra Brachy 4.5 radiation therapy software because incorrect source step sizes may occur in treatment plans.
VIV&LUL is recalling about 950 children's pajama sets sold on Amazon.com because they fail to meet federal flammability standards, posing a risk of burn injuries.
Pharmedium Services, LLC is voluntarily recalling 978 bags of compounded Oxytocin in Lactated Ringer's Injection because the drug was subpotent.
Dondolo is recalling about 3,100 children's nightgowns and pajama sets because they fail to meet federal flammability standards, posing a burn risk.
Sysmex America is recalling Fluorocell PLT reagent lots because they may produce falsely low platelet results, potentially affecting diagnostic accuracy.
Encore Medical is recalling 46 EMPOWR PS Knee Inserts because one unit was packaged with the wrong implant. The recall covers US nationwide distribution.
Encore Medical is recalling 48 units of EMPOWR PS Knee inserts because one unit was packaged with the wrong implant reference number.
Siemens Medical Solutions is recalling 16 torque wrenches used to install Symbia CT scanners because the tools were found to be out of tolerance.
Wockhardt USA is recalling 5mg Enalapril Maleate tablets because they failed impurity specifications. The recall covers 5,050 bottles distributed nationwide.
Teva Pharmaceuticals USA is recalling 58,292 bottles of Methylphenidate Hydrochloride Tablets USP, 20 mg, because they failed to meet dissolution specifications.
Vi-Jon, Inc. is recalling Equate and Studio 35 Clarifying Face Daily Moisturizers because the products failed stability specifications. The recall covers 67,532 bottles distributed nationwide.
Taro Pharmaceuticals is recalling 16,944 tubes of Fluocinonide Gel USP 0.05% because traces of Dapsone were found in the finished product.
KZRV is recalling 2017-2018 Connect recreational trailers with outside kitchens because the 110-volt outlet lacks Ground Fault Circuit Interrupter (GFCI) protection, posing a shock risk.