State
73,833 recalls have nationwide distribution and so reach Tennessee. 7,861 additional recalls listed Tennessee specifically in their distribution scope.
Of the 7,861 recalls naming Tennessee we have scored against our rubric, 1,324 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,974 (25%) are Severe.
Which agencies issued them
These figures cover only the 7,861 recalls whose distribution notice names Tennessee specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
American Surgical Company is recalling 33 boxes of Americot Blue sponges because defective packaging may compromise sterility.
American Surgical Company is recalling 11 boxes of Ultracot sponges because defective packaging may compromise sterility. The products were distributed worldwide.
Akorn, Inc. is recalling ORIS (chlorhexidine gluconate) oral rinse because multiple batches failed impurity specifications.
American Surgical Company is recalling Uniqcot sponges because defective packaging may compromise sterility. The recall covers 15 cases distributed worldwide.
American Surgical Company is recalling 689 boxes of Delicot sponges because defective packaging may compromise sterility.
American Surgical Company is recalling 33 boxes of Delicot-J sponges because defective packaging may compromise sterility.
Sinco is recalling Archer Farms Greek-Inspired Spinach & Feta Cheese Artisan Pizza because a consumer found a small piece of gray plastic in the product.
RaySearch Laboratories is recalling RayStation Therapy Treatment Planning System software due to a bug that can cause views to become unsynchronized with stored data.
Lymol Medical is recalling Sclerosol Intrapleural Aerosol because a defective stem valve may cause the canister to leak propellant, resulting in no drug or an inadequate dose being delivered.
Pfizer is recalling 68,214 bottles of Zoloft 100 mg tablets because some tablets were thicker than specifications. The recall covers nationwide distribution and Puerto Rico.
Synthes (USA) Products LLC is recalling 1,274 sterile 3.2 mm radiolucent drill bits because the protective cap may not be secured, risking puncture of the sterile barrier.
American Surgical Company is recalling 338 boxes of Delicot sponges because defective packaging compromises sterility. The products were distributed worldwide.
Volcano Corporation is recalling specific cardiology imaging systems due to a software incompatibility that can cause unexpected reboots when encountering specific hospital network data.
Synthes (USA) Products LLC is recalling 7,363 sterile 3.2 mm three-fluted drill bits because the protective cap may not be secured, allowing the tip to puncture the sterile barrier.
Akorn, Inc. is recalling Chlorhexidine gluconate oral rinse due to an out-of-specification result for an unknown impurity.
Ford is recalling specific 2005-2011 vehicles because passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.
Stanley Assembly Technologies is recalling specific air-impact wrenches with a software error that may cause over-tightening of vehicle lug nuts, increasing crash risk.
Winnebago is recalling 2015-2016 Tour and Itasca Ellipse motor homes because a steering box defect could cause loss of steering ability.
Broan-NuTone is recalling L500 series ventilation fans because the motor can overheat and cause a fire. No injuries have been reported.
Mirka is recalling approximately 2,500 electric random orbital sanders sold in the U.S. because they can short circuit, posing a fire hazard.
Nissan is recalling 2013-2014 Pathfinder vehicles because an incorrectly installed brake light switch may cause brake lights to stay on or allow shifting out of Park without braking.
Xperion is recalling specific CNG fuel tanks because a neck adapter may pull out, allowing fuel to leak and increasing fire risk.
Forest River is recalling 2015-2016 Glaval Concorde and Concorde II buses because a parking brake cable clip may fail, causing the vehicle to roll unexpectedly.
Jaguar is recalling 2009-2011 XF vehicles in specific states because passenger air bag inflators may rupture during a crash, potentially causing serious injury or death.
Volkswagen Group of America is recalling 2008-2009 Audi A4, A5, and Q5 vehicles because the air bag control units may corrode and fail, potentially preventing air bag deployment in a crash.