State
72,820 recalls have nationwide distribution and so reach Tennessee. 7,818 additional recalls listed Tennessee specifically in their distribution scope.
Of the 7,818 recalls naming Tennessee we have scored against our rubric, 1,317 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,652 (21%) are Severe.
Which agencies issued them
These figures cover only the 7,818 recalls whose distribution notice names Tennessee specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Medline Industries is recalling 71 FEMORAL PACK and FEVAR convenience kits because they contain a potentially contaminated component.
IMRIS Imaging Inc is recalling six ORT200 operating room tables because a mechanical failure could cause unintended movement and patient injury.
Byron White Formulas is recalling its A-FNG Herbal Supplement because the label fails to declare walnuts in English, posing a risk to consumers with nut allergies.
Medline Industries is recalling 15 convenience kits (SKU CDS980375M) due to a potentially contaminated component. The kits were distributed in 18 US states.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium tablets because they may contain less active ingredient than labeled.
Healthmark is recalling ProChek protein tests because they were manufactured with an expired ingredient, which may cause false negative or positive results.
Medline Industries is recalling 94 surgical convenience kits nationwide because they contain a potentially contaminated component.
Philips is recalling Incisive CT scanners with specific software versions due to a potential failure to trigger clinical scans during bolus tracking.
Hollister is recalling specific lots of Onli hydrophilic urethral intermittent catheters because a manufacturing defect may cause a protrusion that leads to genitourinary trauma or bleeding.
Byron White Formulas is recalling its A-P Herbal Supplement because the label fails to declare walnuts in English, posing a risk to individuals with nut allergies.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 125 mcg tablets because they are subpotent. The recall is ongoing nationwide.
Medline Industries is recalling 241 neurosurgical convenience kits distributed nationwide because they contain a potentially contaminated component.
Merge Healthcare is recalling 20 Merge PACS and Merge OrthoPACS workstations because a software issue may cause measurements to be displayed inaccurately.
Medline is recalling 246 surgical convenience kits containing neurosponges due to potential out-of-specification endotoxin levels.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 112 mcg tablets because they are subpotent. The recall covers nationwide distribution.
Medline is recalling 3,468 neurosurgical convenience kits containing Pilling Wecksorb Neurosponges due to potential out-of-specification endotoxin levels.
Henry Schein Inc. is recalling specific lots of Structur 2 SC Temporary Resin Cartridge Refills because they were distributed with incorrect packaging and Instructions for Use.
AVID Medical, Inc. is recalling 130 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.
American Contract Systems Inc is recalling 30 units of Convenience Kits containing Medline catheters because samples failed performance specifications.
American Contract Systems Inc is recalling 12 Convenience Kits containing Medline catheters because samples failed performance specifications.
AVID Medical is recalling 78 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 150 mcg tablets because they may contain less active ingredient than labeled.
AVID Medical is recalling 63 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.
Olympus is recalling 335 PowerSeal 5 mm Sealer & Divider devices because the outer shelf box is incorrectly labeled as a 37-cm device.
Henry Schein Inc. is recalling specific lots of Grandio Universal Nano-Hybrid Restorative Material capsules because they were distributed with incorrect packaging and Instructions for Use.