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.
360 Electrical is recalling three models of surge protectors because they can short circuit when non-grounded plugs are connected, posing a shock or fire hazard.
Rhino Metals is recalling Bighorn P-20 handgun security safes because they can be opened without a combination, posing a serious risk of injury to children and others.
Far East Brokers is recalling about 6,000 children's chairs and swings because the screen-printing contains excessive lead, violating federal standards. No injuries have been reported.
Southeast Toyota Distributors is recalling 2015-2016 Toyota and Scion vehicles because the load carrying capacity label may be incorrect, potentially leading to vehicle overload.
Volkswagen Group of America is recalling 2007-2009 Audi A8 and S8 vehicles because the sunroof glass may not be properly secured and could detach while driving.
The Kroger Co is recalling Roasted & Salted Sunflower Kernels due to potential Listeria monocytogenes contamination.
The Kroger Co is recalling Salted Sunflower Kernels because the supplier notified the firm that the product may be contaminated with Listeria monocytogenes.
The Kroger Co is recalling Cranberry Delight Trail Mix because it may be contaminated with Listeria monocytogenes.
Integra LifeSciences is recalling 2,487 MicroFrance electrosurgical instruments due to reports of unintended patient or operator burns and electric shock.
Akorn, Inc. is recalling specific lots of Sulfacetamide Sodium Ophthalmic Solution because they failed antimicrobial effectiveness testing, raising concerns about sterility.
Invisiblu International LLC is recalling LGD-Xtreme capsules containing unapproved ligandrol because the product was marketed without an approved NDA or ANDA.
FDA is recalling Curity All Purpose Sponges due to compromised sterility from a barrier breach. The recall affects units distributed in the US and 20 other countries.
Covidien LLC is recalling Vistec X-Ray Detectable Sponges because a breach of the barrier packaging may have compromised sterility.
The FDA is recalling Curity X-Ray Detectable Laparotomy Sponges because a breach of the barrier packaging may have compromised their sterility.
Covidien LLC is recalling Curity Gauze Sponges because a breach of the barrier packaging may have compromised their sterility.
Forest River is recalling 2015 Glaval Synergy transit buses because steering boxes may wear prematurely, risking loss of steering control.
The FDA is recalling Curity X-Ray Detectable Laparotomy Sponges because a breach of the barrier packaging may have compromised their sterility.
Liquid Assets Inc. is recalling Angel Wings and Magzuma dietary supplements because they contain undeclared milk and soy allergens.
FDA is recalling Curity X-Ray Detectable Laparotomy Sponges due to compromised sterility from a barrier breach.
Newmar is recalling 2014-2016 Dutch Star motorhomes because a defective steering box may cause loss of steering control.
Terex Advance is recalling 338 model year 2016 Front Discharge Concrete Mixer trucks because a weld failure could cause the main chute to detach while driving, increasing crash risk.
The FDA is recalling Curity X-Ray Detectable Laparotomy Sponges because a breach of the barrier packaging may have compromised their sterility.
The FDA is recalling Curity X-Ray Detectable Laparotomy Sponges due to compromised sterility caused by a breach of the barrier.
Pentax Medical is recalling 423 Video Duodenoscopes nationwide after reports of carbapenem-resistant Enterobacteriaceae (CRE) infection at a medical facility.
FDA is recalling Kerlix X-Ray Detectable Laparotomy Sponges due to compromised sterility from a barrier breach.