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.
Wescam Inc is recalling 29 MX-10 surveillance laser systems because the ocular hazard distance is longer than specified, posing a risk of eye exposure.
Ethicon is recalling specific Proline suture products because a packaging design issue allows needles to perforate the package, posing injury and infection risks.
Siemens is recalling 197 units of Dimension Vista MULTI 1 SDIL diluent due to a potential defect in the vial cap septum that may cause inaccurate test results.
NewDeal SA is recalling TIBIAXYS devices because use may cause superficial or deep infections requiring antibiotic treatment or device removal.
T R Toppers, Inc. is recalling Chopped Chocolate Pretzel Pieces due to potential peanut contamination. Consumers should check for Lot 10481 and stop using the product.
Ethicon is recalling 300 units of Proline Suture 30" 6-0 Blue because a packaging design issue may allow the needle to perforate the package, posing injury or infection risks.
Opgen Inc is recalling AdvanDx QuickFISH Slides because they may show diminished performance before their expiration date.
Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
The Hain Celestial Group is recalling alba BOTANICA sport mineral sunscreen because the wrong product formulation was placed in the packages.
Philips is recalling 32 Ingenuity Digital PET/CT Systems because a block connecting the patient pallet to the couch may be assembled incorrectly, potentially causing a misaligned screw.
Cardinal Health is recalling Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
Stryker is recalling 180 reprocessed Harmonic Ace shears because they may display an error code preventing use.
Siemens Healthcare Diagnostics is recalling 1,446 units of Dimension Vista CTNI Sample Diluent because a defective cap septum may cause erroneously elevated test results.
Valeris Medical is recalling 113 Apollo XT Suture Anchors because the labels incorrectly identified the material as titanium instead of PEEK.
Fx Solutions is recalling specific proton beam therapy heads due to a breach in the external blister packaging.
Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
Fx Solutions is recalling specific lots of Humelock Offset Heads due to a breach in the external blister packaging.
Intel-GE Care Innovations LLC is recalling the Health Harmony Mobile application because patient data sometimes failed to sync with the backend database in a timely manner.
Siemens is recalling 1,195 units of Dimension Vista MULTI 2 SDIL diluent because a defective septum may cause erroneously elevated test results.
Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
SynTec is recalling S3B 45-inch Restraint School Bus Seats because the mounting foot may pull through the bolted joint at the bus floor, increasing injury risk in a crash.
JCPenney is recalling Okie Dokie Denim Patches Shortie shorts because the patches can detach, posing a choking hazard to young children.
Ross Stores is recalling Bronze Hammered bistro chairs because the frames can break, posing a fall hazard. Consumers should stop using the chairs and return them for a full refund.
Karma Automotive is recalling 2018 Revero vehicles because the driver's side exterior rearview mirror may use convex glass instead of flat glass, failing federal safety standards.
Meritor is recalling specific wheel studs installed in steer axle hubs because improper heat treatment may cause them to fail, potentially leading to wheel detachment.