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.
Aurobindo Pharma USA Inc is recalling 47,040 bottles of Venlafaxine Hydrochloride extended-release capsules because some contain punctured or clumped capsules.
Yum Restaurants International is recalling Pizza Hut Creamy Alfredo sauce due to a likely flexible plastic foreign object.
Atrium Medical Corporation is recalling 1,394 cases of 10 Fr Straight Thoracic Catheters because the label icon incorrectly depicts six eyelets instead of two.
Philips is recalling BrightView XCT systems because the intended use in the instructions for use did not match the 510K submission.
Philips Medical Systems is recalling 425 BrightView XCT systems because the intended use listed in the instructions for use did not match the 510K submission.
Actavis Inc is recalling specific lots of Glipizide extended-release tablets because they failed to meet dissolution specifications at the 10-hour testing point.
Siemens is recalling CentraLink Data Management System software versions v13x, v14x, and v15x because the system may download orders to the ADVIA Automation System without specifying the sample type.
Becton Dickinson is recalling specific lots of BD Vacutainer blood collection tubes because they contain approximately twice the expected amount of buffered sodium citrate additive.
Teva Pharmaceuticals USA is recalling specific lots of Mimvey Lo tablets because they failed impurity specifications for norethindrone.
Greatbatch Medical is recalling 1,441 T5766 Offset Reamer Handles because the drive chain U-joints may seize during hip surgery, rendering the device non-functional.
Atrium Medical Corporation is recalling 8 Fr Straight Thoracic Catheters because the label depicts six eyelets instead of the correct two.
Accord Healthcare is recalling 12,896 bottles of 5 mg Lisinopril tablets because the tablets are missing a break line. The recall covers the U.S. and Puerto Rico.
Argon Medical Devices is recalling 15 boxes of Harvest Needles because a potential defect in the blister packaging may compromise the sterility of the product.
LEO Pharma Inc. is recalling Taclonex topical suspension because it was packaged with an out-of-date package insert.
NOW Foods is recalling Multi-Food 1 Tablets because the label incorrectly states the molybdenum content is 75 mg instead of 75 mcg.
Yamaha is recalling 2015-2016 YZF-R3 motorcycles because engine vibration may cause the fuel tank bracket to contact the tank, potentially leading to a fuel leak and fire risk.
LiquidSpring is recalling certain Compressible Liquid Adaptive Suspension Systems because overtightened rear brake banjo bolts may cause loss of rear brakes, increasing crash risk.
Yamaha Corporation of America is recalling about 900 piano benches sold with grand pianos because the interior paint contains excessive lead, violating federal standards.
SodaStream is recalling about 51,000 one-liter carbonating bottles because they can burst under pressure, posing an injury hazard to users and bystanders.
Yamaha is recalling 2015-2016 YZF-R3 motorcycles because water can corrode the ignition switch, causing the engine to stall unexpectedly and increasing crash risk.
Winnebago is recalling 2016-2017 Travato recreational vehicles because the liquid propane hose may contact the emergency brake cable, potentially causing a propane leak that increases the risk of fire or explosion.
Autoliv is recalling AI2 Air Bag Initiators manufactured between June 2016 and November 2016 because an improper chemical mix may prevent air bags from deploying properly in a crash.
Roush CleanTech is recalling propane conversion kits for Ford F-250 trucks because worn fittings may cause a propane leak, increasing fire risk.
Altec is recalling 2015-2016 AH125, AH150, and HL125 aerial devices because rotation bearing fasteners may fail, posing a risk of injury or death.
Altec Industries is recalling 2016 DLB Digger Derrick vehicles because fasteners securing the outer rotation bearings may fail, potentially causing the boom to move unintentionally.