State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Palmer and Company is recalling 198 cases of Palmer's Candies Chocolatey Pretzels because an ingredient may be contaminated with Salmonella.
Biomet U.K. is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Hospira is recalling 578,784 bags of Metronidazole Injection due to a customer report of a leaking bag, which compromises sterility assurance.
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Biomet is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Tosoh Bioscience is recalling 682 HLC-723G8 analyzers because they may report inaccurate HbA1c values for patients with specific hemoglobin variants.
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Pier 1 Imports is recalling about 363,000 glass knobs sold in the U.S. because they can break and cause lacerations.
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Arrow International Inc is recalling 215,703 vascular catheter introduction kits nationwide because complaints were received regarding peel away sheaths flaring.
Biomet U.K., Ltd. is recalling Oxford Knee System Tibial Resector Body Tubes and Guides due to potential alumina inclusions that could cause the instruments to crack or separate.
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Falafel King is recalling 1,380 containers of Tzatziki Sauce due to undeclared milk on the label. The product was distributed in Colorado, New Mexico, Utah, and Nebraska.
Biomet U.K., Ltd. is recalling Oxford Unicompartmental Knee Phase 3 Shim Size 1 instruments due to potential alumina inclusions that could cause cracking and separation.
Biomet is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Volvo is recalling 2017 S60, V60, and XC60 vehicles because side air bag inflators may fail to ignite, preventing deployment in a crash.
Biomet U.K., Ltd. is recalling Oxford Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Biomet U.K., Ltd. is recalling Oxford Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Biomet is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Biomet is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Forest River is recalling 2017 Rockwood and Flagstaff recreational trailers because a slide room bracket may damage the front tire, causing deflation and increasing crash risk.
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Biomet U.K., Ltd. is recalling Oxford Unicompartmental Knee Phase 3 Shim Size 3 instruments due to potential alumina inclusions that could cause cracking and separation.