State
73,741 recalls have nationwide distribution and so reach New York. 12,955 additional recalls listed New York specifically in their distribution scope.
Of the 12,955 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 12,955 recalls whose distribution notice names New York specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
RemedyRepack Inc. is recalling specific lots of Ranitidine 150 mg tablets because the supplier reported potential Nitrosodimethylamine (NDMA) levels above established limits.
Vactor is recalling 2017-2020 2100i vehicles because a software defect may cause safety interlocks to fail, leading to unintentional vehicle movement and increased crash risk.
Akoury is recalling Boss67 motorcycle helmets that may lack proper impact protection, increasing the risk of injury in a crash.
Siemens is recalling ADVIA Centaur Folate test kits because homocysteine assays may cause elevated folate results.
Evenflo is recalling about 3,100 Pillo Portable Napper inclined sleepers due to a risk of infant suffocation. Consumers should stop using the product immediately and contact Evenflo for a refund.
Isopure Corp is recalling eight Finish Thompson Centrifugal Pumps due to a manufacturing defect that could expose magnets to solution, causing corrosion and iron contamination.
Polymer Technology Systems is recalling 44,448 CardioChek Plus Professional Analyzers because a battery terminal defect can cause overheating if batteries are inserted incorrectly.
Kovatch Mobile Equipment is recalling specific KME Predator emergency vehicles because flashlight battery packs may explode while charging, increasing injury risk.
Polymer Technology Systems is recalling 44,448 Henry Schein CardioChek Starter Kits because a battery terminal defect can cause overheating if inserted incorrectly.
Summer Infant is recalling about 46,300 SwaddleMe By Your Bed inclined sleepers to prevent the risk of infant suffocation. Consumers should stop using the product immediately and contact the company for a refund.
Isopure Corp is recalling 15 Acidified Concentrate Distribution and Storage Systems due to a potential magnet encapsulation defect that could cause corrosion and iron exposure.
Polymer Technology Systems is recalling 44,448 refurbished CardioChek Plus Professional Analyzers because a battery terminal defect may cause overheating if batteries are inserted incorrectly.
Beckman Coulter is recalling iChem VELOCITY Urine Chemistry Analyzers because a software issue may prevent specific gravity flags, potentially leading to erroneous test results.
GE Healthcare is recalling Centricity Universal Viewer 6.0 because incorrect measurements in DICOM files may lead to potential misdiagnosis.
Isopure Corp is recalling one IsoMix PRO system due to a potential magnet encapsulation defect that could cause corrosion and iron exposure.
Delta Enterprise Corp. is recalling about 5,900 incline sleepers for newborns to prevent the risk of suffocation. Consumers should stop using the products immediately.
Graco is recalling Little Lounger Rocking Seats to prevent the risk of infant suffocation. Consumers should stop using the product and contact Graco for a refund.
Paltop Advanced Dental Solutions is recalling 67 dental implants because some were packaged with the wrong cover screw, preventing proper fit.
Acclarent, Inc. is recalling three lots of TruDi NAV Suction Instruments because calibration issues cause incorrect tip orientation displays.
Medicrea International is recalling 190 units of Pass LP Blunt K-wires because they may not fit into Conical Cannulated Screws.
Acclarent, Inc. is recalling TruDi NAV Suction Instruments because calibration issues cause incorrect tip orientation displays.
Acclarent, Inc. is recalling specific lots of TruDi NAV Suction Instruments because calibration issues cause incorrect tip orientation displays.
Siemens is recalling 3,627 ADVIA Centaur Folate test kits because homocysteine assays may cause elevated folate results.
Medicrea International is recalling 30 units of Pass LP Trocar K-wires because they may not fit into conical cannulated screws.
Hikma Pharmaceuticals is recalling 4,840 vials of Methylprednisolone Sodium Succinate Injection because the label incorrectly instructs healthcare professionals to reconstitute the product with 16 mL instead of 8 mL.