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.
R Thomas Marketing, LLC is recalling Super Hard capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
R Thomas Marketing, LLC is recalling Herb Viagra because it was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
R Thomas Marketing, LLC is recalling Real Skill capsules because the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
American Surgical Company is recalling 34 boxes of strung cotton balls due to packaging defects that compromise sterility. The products were distributed worldwide.
R Thomas Marketing, LLC is recalling African Black Ant capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
R Thomas Marketing, LLC is recalling Zhong Hua Niu Bian capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
R Thomas Marketing, LLC is recalling Man King capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Fresenius Kabi USA is recalling Octreotide Acetate Injection vials because they failed impurities and degradation specifications.
R Thomas Marketing, LLC is recalling Plant Vigra because it was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
R Thomas Marketing, LLC is recalling Night Man capsules because the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
R Thomas Marketing, LLC is recalling Black Storm capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
R Thomas Marketing, LLC is recalling Bull's Genital capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Volkswagen Group of America is recalling specific Audi A4 and A6 models because passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.
M.B. Sturgis is recalling specific propane gas regulators where a cracked window may allow gas to leak, increasing fire risk. Dealers will replace the parts free of charge.
The Sausage Maker, Inc. is recalling Smoked Pepperoni seasoning because the Fermento ingredient contains undeclared whey protein and skim milk powder.
The Sausage Maker, Inc. is recalling Goetburg Summer Sausage seasoning due to undeclared whey protein and skim milk powder.
Akorn, Inc. is recalling PerioRx oral rinse because multiple batches failed impurity specifications. The product contains an unknown impurity of chlorhexidine gluconate.
Teva North America is recalling 546 bags of Linezolid Injection due to potential leaking that compromises sterility.
R Thomas Marketing, LLC is recalling Zhen Gong Fu capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
The FDA is recalling Black Ant supplements distributed by R Thomas Marketing, LLC because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Southwire is recalling approximately 1.2 million non-contact voltage detectors because they may provide false readings, posing shock and burn risks.
Mohu is recalling about 1,700 BeBox smart boomboxes because they can overheat, posing burn and fire hazards. One incident of a unit catching fire was reported, with no injuries.
R Thomas Marketing, LLC is recalling Bull capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Traxxas is recalling X-Maxx Monster Trucks and VXL-6 electronic speed controls because a short circuit can cause a fire. The company reported 40 fires and one injury.
American Surgical Company is recalling Delicot X sponges due to packaging defects that compromise sterility. The recall covers 3 boxes distributed worldwide.