State
73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Red Mountain Compounding Pharmacy is recalling S-Atropine 0.02% ophthalmic solution due to a lack of assurance of sterility. The affected product is a prescription eye drop distributed nationwide.
Mystery Ranch is recalling Quick Draw Side Arm Holsters because the retention strap can disconnect, allowing the handgun to fall and unexpectedly discharge.
Western / Scott Fetzer Company is recalling 6,790 Grab n Go Opti series VIPR systems because the control knob may rotate beyond its functional range, limiting access to flow settings.
Argon Medical Devices is recalling 49,130 AHD Luer Lock Caps because an incomplete seal may cause loss of sterility.
Western / Scott Fetzer Company is recalling 1,287 Grab n Go Opti VIPR oxygen delivery systems because the control knob may rotate beyond its functional range, limiting access to flow settings.
Red Mountain Compounding Pharmacy is recalling specific lots of Testosterone Cypionate 100mg/mL in sesame oil due to a lack of assurance of sterility.
Cold Locker Processing LLC is recalling 2,520 lbs of Kroger Wild Caught Sockeye Salmon due to potential Listeria monocytogenes contamination.
Argon Medical Devices is recalling specific stopcock products because incomplete pouch seals may cause a loss of sterility.
Red Mountain Compounding Pharmacy is recalling S-Sodium Selenite 0.219% injections because the agency could not ensure the product was sterile.
Argon Medical Devices is recalling 49,130 units of TRI-JECT 3 Way IV Administration Organizers because an incomplete seal may cause loss of sterility.
Argon Medical Devices is recalling specific lots of Luer Lock Plugs because an incomplete seal may cause a loss of sterility.
Centurion Medical Products is recalling 80 units of Universal Line Full Body Drape Kits due to incomplete sterile packaging seals that may compromise product sterility.
Baxter Healthcare is recalling 336 Prismaflex Control Units with software versions below 7.21 due to communication error alarms that may interrupt therapy or cause blood loss.
Western / Scott Fetzer Company is recalling 25,840 Grab n Go Opti VIPR systems because the control knob may rotate beyond its functional range, limiting access to flow settings.
Becton Dickinson is voluntarily recalling MaxZero Extension Sets with Needle-less Connectors because fluid droplets may separate from the sealed surface after disconnection.
Zimmer Biomet is recalling 5,459,583 periarticular shoulder plates because non-highly polished implants may adhere to the LDPE bag packaging.
Argon Medical Devices is recalling Septishield II products because an incomplete seal may cause a loss of sterility.
Argon Medical Devices is recalling Hemostasis Valves because incomplete pouch seals may cause a loss of sterility.
Argon Medical Devices is recalling Vascuclamp radiopaque vascular clamps because an incomplete pouch seal may cause a loss of sterility.
Argon Medical Devices is recalling Double Male LL Adapters because an incomplete pouch seal may cause a loss of sterility.
Hitachi Medical Systems America Inc is recalling 39 Scenaria Whole-body X-ray CT Systems because cables to the controller unit may not be affixed properly, creating a risk of detachment during scanning.
Zimmer Biomet is recalling cable buttons for NCB Polyaxial Locking Plates because non-highly polished implants may adhere to the packaging bag.
Ortho-Clinical Diagnostics is recalling VITROS K+ Slides because a mechanical failure may cause intermittent slide dispense issues.
Western / Scott Fetzer is recalling 143,164 Grab n Go Opti VIPR oxygen systems because the control knob may rotate beyond its functional range, limiting access to flow settings.
Zimmer Biomet is recalling 5.4 million tibial plates because non-highly polished implants may adhere to the packaging bag.