State
73,716 recalls have nationwide distribution and so reach Tennessee. 7,859 additional recalls listed Tennessee specifically in their distribution scope.
Of the 7,859 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 1,973 (25%) are Severe.
Which agencies issued them
These figures cover only the 7,859 recalls whose distribution notice names Tennessee specifically. The 73,716 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Par Health USA is recalling 18,991 vials of Argatroban Injection because they contain particulate matter. The affected vials were distributed nationwide.
AVID Medical is recalling 80 Halyard Anterior Hip Packs because a non-sterile component was not properly sterilized.
Ventec Life Systems is recalling 180 ventilator units because an internal cable connector may disconnect, causing system reboots and interruption of ventilation therapy.
Ventec Life Systems is recalling 930 ventilators because an internal cable may disconnect, causing system reboots and therapy interruption.
Ventec Life Systems is recalling 4,369 VOCSN+Pro ventilators because an internal cable connector may disconnect, causing system reboots and interruption of therapy.
Ventec Life Systems is recalling VC+Pro ventilators because an internal cable connector may disconnect, potentially interrupting ventilation therapy.
Techno-Path is recalling Multichem AE Unassayed Level 3 quality control material because stability drift affects the Ammonia analyte, potentially delaying diagnostic results.
Par Health USA, LLC is recalling 1,944 vials of Argatroban Injection due to the presence of particulate matter in the solution.
Medtronic is recalling CareLink Clinic software version 4.4A because a defect in the Settings Calculator feature may result in incorrect rapid-acting insulin parameters.
AVID Medical, Inc. is recalling 56 Halyard Anterior Hip Packs because a non-sterile component was not properly sterilized.
Ventec Life Systems is recalling 100 units of ventilator parts because the internal flow transducer cable connector may disconnect, potentially interrupting ventilation therapy.
Medtronic is recalling the MiniMed Go app version 1.2.1 because a software defect prevents long-acting insulin dose reminders from appearing, potentially leading to missed or duplicate doses.
Right Value Drug Stores LLC is recalling 4,675 vials of compounded Testosterone Cypionate due to a lack of sterility assurance.
Pfizer is recalling 134 bottles of Levoxyl (levothyroxine sodium) 175 mcg tablets due to confirmed subpotency. The product was distributed nationwide and in Puerto Rico.
Ventec Life Systems is recalling 1,532 VOCSN ventilator parts because an internal cable connector may disconnect, potentially interrupting ventilation therapy.
Ventec Life Systems is recalling V+Pro ventilators because an internal cable may disconnect, causing system reboots and interruption of therapy.
Ventec Life Systems is recalling VC+Pro ventilators because an internal cable may disconnect, causing system reboots and interruption of therapy.
Ember is recalling 2024 E-Series travel trailers because the power cord fuse may not provide adequate circuit protection, increasing the risk of a fire.
Techno-Path is recalling Multichem AE quality control material because stability drift affects the Ammonia analyte, potentially delaying diagnostic results.
Beckman Coulter is recalling 92 Optima ultracentrifuge rotors that may break during operation, potentially destroying samples and exposing personnel to biohazards.
Medline Industries is recalling specific medical convenience kits because they are difficult to remove and leave adhesive residue on patient skin.
Boston Scientific is recalling 382 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Medline is recalling 108 C-Section Tray kits because they are difficult to remove from patients and leave adhesive residue on the skin.
Medtronic is recalling InterStim SureScan MRI Leads because selecting an incompatible lead or extension prevents the system from working as intended.
Medline Industries is recalling 10 FETOSCOPY CDS-LF medical convenience kits because they are difficult to remove from patients and leave adhesive residue on the skin.