State
73,817 recalls have nationwide distribution and so reach Tennessee. 7,860 additional recalls listed Tennessee specifically in their distribution scope.
Of the 7,860 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 7,860 recalls whose distribution notice names Tennessee specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Arctic Cat is recalling 2017 Wildcat ROVs and winch kits because the winch solenoid can overheat and cause fires. No injuries have been reported.
BMW is recalling 2014-2018 i3 vehicles because unbelted, small adult drivers face a higher risk of neck injury in frontal crashes.
Smeal is recalling 2013-2017 Aerial and Pumper fire apparatus because corroding rings may cause pressure relief valves to open, reducing water pressure.
Spartan Motors is recalling 2014-2017 Gladiator and MetroStar emergency vehicles because corroded rings may cause pressure relief valves to open, reducing water pressure for firefighting.
Precision Shooting Equipment Inc. is recalling approximately 17,000 archery crossbows because they may fire unexpectedly, posing an injury risk to users and bystanders.
Purdue Pharma is recalling Betadine Povidone-Iodine swabsticks because a manufacturing error caused the product to be subpotent.
Toyota is recalling 2012-2015 Prius Plug-in Hybrids because a fuse may fracture, causing power loss and increasing crash risk.
BMW is recalling 3,188 2018 vehicles because a software error may prevent the instrument panel from illuminating, increasing crash risk.
Teleflex Medical is recalling 13,710 units of the Auto Endo5 Automatic Hem-o-lok Clip Applier because clips may misalign, jam, or fall out of the device.
21st Century Snack Foods is recalling Dark Chocolate Almonds because the product contains undeclared milk, a major food allergen.
Bush Hog is recalling about 500 HDE riding lawn mowers because the blade can separate from the spindle, posing a laceration hazard.
Terumo BCT is recalling 525 Harvest Graft Delivery Packs because some lots may lack a seal on the inner pouch, potentially compromising sterility.
Toyota is recalling 2018 C-HR vehicles because the electronic parking brake may fail to engage or disengage, increasing the risk of vehicle rollaway.
Sorin Group USA is recalling a specific lot of FlexFlow Venous Cannulas because they are sharper or pointier than expected.
Encore Medical is recalling 840 units of Cobalt MV Bone Cement because the sterile Tyvek packaging seal may be lost, potentially compromising sterility.
Wholesale Fireworks is recalling Toxic artillery rockets, Boom Box aerial shells, and Detonator firecrackers due to federal standard violations that pose explosion and burn hazards.
Epimed International is recalling 500 units of RX-2 COUDE Epidural Needles due to a potential incomplete seal that may impact sterility.
Encore Medical, Lp is recalling Cobalt HV with Gentamicin bone cement because the sterile Tyvek packaging may have lost its seal, potentially compromising sterility.
Epimed International is recalling 263 units of TUOHY Epidural Needles because a partially incomplete seal could impact the product's sterility.
Becton Dickinson is recalling 90,000 blood collection tubes due to incorrect labeling at the case and shelf pack level.
Encore Medical, Lp is recalling 1,815 units of Cobalt MV with Gentamicin bone cement because the sterile Tyvek packaging seal was lost.
Encore Medical is recalling Biomet Cobalt HV Bone Cement because the sterile Tyvek packaging seal may be lost, potentially compromising sterility.
Aaren Scientific Inc. is recalling 786 boxes of AERO IOL Injection Systems because the recommended storage temperature on the label is incorrect.
Northgate Technologies is recalling 186 electrohydraulic lithotripter probes due to incorrect reference numbers on labels, which could delay patient care.
Invivo Corporation is recalling 529 Xper Flex Cardio PhysioMonitoring systems because of intermittent communication issues between the host system and the device.