State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Wegmans is recalling store-made shrimp salad sold in several states due to potential Listeria monocytogenes contamination.
Shyft Group is recalling 2020 Utilimaster Metris vehicles because the payload capacity on the Tire and Loading Information label may be higher than the actual capacity, increasing the risk of tire failure and crashes.
Wegmans is recalling Ready to Cook Whole Soft Shell Crab with Lemon due to potential Listeria monocytogenes contamination. Consumers should check their refrigerators for this product.
Wegmans is recalling Bay Seasoned Soft Shell Crab potentially contaminated with Listeria monocytogenes. Consumers should discard or return the product.
Ultimate Leather is recalling Zone HS1100 motorcycle helmets manufactured between 2014 and 2016 because they may not adequately protect the wearer in a crash.
Datascope Corporation is recalling Intra-Aortic Balloon Catheters due to potential endotoxin contamination. The recall covers kits distributed worldwide.
Datascope is recalling 32,855 Intra-Aortic Balloon Catheter kits due to potential endotoxin contamination. The affected products were distributed worldwide.
Wegmans Food Markets is recalling Lobster Claw and Shrimp Platters sold in six states due to potential Listeria monocytogenes contamination.
Ortho Clinical Diagnostics is recalling VITROS XT3400 Chemistry Systems because slides in Slot 18 may be mis-positioned, leading to erroneous test results.
Wegmans is recalling AIP Veggie Pizzas in several states because they may be contaminated with Listeria monocytogenes.
Datascope Corporation is recalling 2,550 kits of Trans-Ray 7Fr 34cc Intra-Aortic Balloon Catheters due to potential endotoxin contamination. The affected devices were distributed worldwide.
Karl Storz is recalling 2,083 flexible intubation video endoscopes to provide updated sterilization instructions. The update prevents the use of specific trays and ethylene oxide sterilization to avoid introducing infectious agents into patient airways.
Wegmans Food Markets is recalling specific chicken cutlets sold in the Northeast and Mid-Atlantic regions due to potential Listeria monocytogenes contamination.
Klarity Medical Products LLC is recalling 111 vacuum bags used for patient positioning during radiation therapy because they may not hold a vacuum adequately for the required treatment time.
Wegmans Food Markets is recalling seasoned whole rainbow trout potentially contaminated with Listeria monocytogenes. Consumers should check their refrigerators and discard or return the product.
Neurovision is recalling Cobra x5 EMG endotracheal tubes because the electrode insulation may soften and damage, potentially stopping EMG signal transmission.
Neurovision is recalling Cobra x5 2-Ch EMG ET Tubes because the electrode insulating material may soften over time, potentially damaging the device and stopping EMG signal transmission.
Wegmans Food Markets is recalling fresh cooked shrimp and crab claw trays due to potential Listeria monocytogenes contamination. Consumers should not eat the product.
Datascope Corporation is recalling 6,111 Intra-Aortic Balloon Catheter kits due to potential endotoxin contamination. The affected products were distributed worldwide.
Wegmans is recalling Whole Seasoned Snapper sold in several states because it may be contaminated with Listeria monocytogenes.
Datascope is recalling Intra-Aortic Balloon Catheters due to potential endotoxin contamination. The recall affects 1,746 kits distributed worldwide.
Siemens is recalling Cios Alpha and Cios Spin mobile X-ray systems because a hardware error could cause permanent loss of imaging functionality.
Neurovision is recalling Nerveana x5 RLN Monitoring Kits because the electrode insulating material may soften, potentially stopping EMG signal transmission and rendering the device unusable.
Neurovision Medical Products Inc. is recalling Nerveana x5 RLN Monitoring Kits because the electrode insulating material may soften, potentially stopping EMG signal transmission and rendering the device unusable.
Siemens Medical Solutions is recalling E.cam and Symbia systems with foresight detectors because they may lose detector time information during gated or dynamic acquisitions.