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.
Cargill is recalling Beyond Premium Liquid Butter Alternative due to excessive amounts of TBHQ and dimethyl polysiloxane.
First Source LLC is recalling Hikers Haven Trail Mix due to potential Listeria monocytogenes contamination. The product was distributed in 11 states.
Cantrell Drug Company is recalling 645 vials of Calcium Chloride Injection Solution because the firm cannot assure the sterility of the product.
Cantrell Drug Company is recalling 1,748 bags of Morphine Sulfate 1 mg/mL due to a lack of assurance of sterility. The product was distributed nationwide.
Ohio Hickory Harvest Brand Products Inc. is recalling 25 lb. bags of Rucker's Cajun Mix due to potential Listeria monocytogenes contamination.
Cantrell Drug Company is recalling 935 vials of Hydromorphone HCl 50 mg/50 mL single-dose syringes due to a lack of assurance of sterility.
Cantrell Drug Company is recalling 80 bags of Calcium Chloride 1 g/50 mL due to a lack of assurance of sterility.
Cantrell Drug Company is recalling 30,796 syringes of Phenylephrine HCl 1 mg/10 mL due to a lack of assurance of sterility. The recall covers products distributed nationwide.
Cantrell Drug Company is recalling specific lots of Neostigmine Methylsulfate injection syringes because the firm cannot ensure the products are sterile.
Cantrell Drug Company is recalling 2,681 bags of Oxytocin 30 USP Units due to a lack of assurance of sterility. The affected product is distributed nationwide.
Cantrell Drug Company is recalling 162 syringes of Lidocaine HCl 1% because the firm cannot assure the sterility of the product.
First Source LLC is recalling specific lots of Oriental Snack Mix due to potential Listeria monocytogenes contamination. The product was distributed to retail stores in 11 states.
Cantrell Drug Company is recalling 93 vials of Hydromorphone HCl injection solution nationwide due to a lack of assurance of sterility.
Apple Tree Goat Dairy is recalling all lots of its 8 oz and 5 lb Chevre products due to potential Listeria monocytogenes contamination.
First Source LLC is recalling multiple varieties of Fitness Mix due to the potential for Listeria monocytogenes contamination. The product was distributed to retail stores in 11 states.
Cantrell Drug Company is recalling 73 bags of Calcium Chloride in 0.9% Sodium Chloride due to a lack of assurance of sterility.
Cantrell Drug Company is recalling specific lots of Succinylcholine Chloride 200 mg/10 mL injection syringes because the firm cannot ensure the products are sterile.
Cantrell Drug Company is recalling 87 bags of Ropivacaine HCl 0.25% due to a lack of assurance of sterility. The product is intended for epidural use only.
Becton Dickinson is recalling specific lots of BD Vacutainer Push Button Blood Collection Sets because the front and rear barrels may separate when the safety feature is activated.
Inovo, Inc. is recalling 117 Inovo Purefill Oxygen Compressor Model PF1100 units because the device can fail during operation.
Steris Corporation is recalling 63 Harmony Insight Diagnostic Monitor Support Systems because spring arm screws may not be properly secured and could become loose.
JFC International is recalling You-ka Fresh Ramune candy because it may contain undeclared wheat. Consumers with wheat allergies should not consume the product.
Stryker is recalling 40,476 reprocessed Xcel Bladeless Trocars because the adjustable plug may break in packaging or during use.
Volvo is recalling 2017 S60, V60, and XC60 vehicles because side air bag inflator initiators may fail to ignite during a crash, preventing deployment.
Toyota is recalling 2017 86 vehicles with automatic transmissions and ignition keys because the key may be removed without the transmission in Park, increasing the risk of the vehicle rolling away.