State
73,718 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 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
New Flyer is recalling certain 2013-2021 electric buses because firmware errors in the inverters may cause the electric drive system to shut down, increasing the risk of a crash.
Medtronic is recalling Bio-Console 560 devices because an electrical component may fail, causing the pump to stop and potentially producing smoke or a burning odor.
Utility Trailer is recalling 2006-2021 VS2DC, VS2DX, and VS3DX trailers because a missing weld may cause the slider rail to detach, increasing crash risk.
Siemens is recalling 1,172 ACUSON Sequoia ultrasound systems because a software error may calculate incorrect Estimated Dates of Delivery, potentially influencing clinical decisions.
Nuvasive Specialized Orthopedics is recalling PRECICE STRYDE intramedullary nails due to complaints of adverse events potentially related to biological safety, including pain and bony abnormalities.
Epicure is recalling glass prep bowls that may shatter during use, posing a laceration hazard. Consumers should stop using the product and contact Epicure for a free replacement.
Ferring Pharmaceuticals is recalling 301 ZOMA-Jet 5 Demonstration Kits because the injector pen may break apart and disintegrate into pieces.
Land O'Lakes is recalling Queso Bravo White Cheese Dip because it may contain metal foreign material. Consumers should stop using the product.
RH is recalling approximately 55,700 children's bath wraps in the U.S. because they fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries.
Nuvasive Specialized Orthopedics is recalling 226 Precice Bone Transport nails due to complaints of pain and bony abnormalities related to biological safety.
Alcon is recalling 249,853 custom ophthalmic surgical procedure packs because mold was found on gowns included in the packages.
Diasorin Inc. is recalling LIAISON 1-84 PTH Assay kits because the system may produce falsely elevated parathyroid hormone results.
Nuvasive Specialized Orthopedics Inc is recalling 40 PRECICE Plate units worldwide due to complaints of adverse events potentially related to biological safety.
Hollister Incorporated is recalling Vertical Drain Tube Attachment Devices (VTAD) because the tube holder can separate from the securing barrier, risking tube migration or loss.
Ferring Pharmaceuticals is recalling 1,569 ZOMA-Jet 10 Demonstration Kits because the injector pen may break apart and disintegrate into pieces.
DePuy Orthopaedics is recalling specific lots of the LCS COMPLETE P.F.C. SIGMA RP Mobile Bearing Total Knee System because of potential damaged packaging.
Oscor, Inc. is recalling 500 units of the AngioDynamics SafeSheath ULTRALITE 10F due to a potential open seal on the sterile product.
Stryker is recalling 102 units of Harmonic ACE +7 Shears because they were distributed without receiving regulatory clearance.
LumiraDx is recalling 2,186 coronavirus antigen test strips because two lots failed quality control testing and produced false positives.
DePuy Orthopaedics is recalling 355 units of the ATTUNE Rotating Platform Total Knee System due to potential damaged packaging. The affected tibial bases are used in cemented total knee arthroplasty.
DePuy Orthopaedics is recalling ATTUNE and MBT tibial base components used in knee replacements due to potential damaged packaging.
Cardinal Health Inc. is voluntarily recalling 48 boxes of Tremfya (guselkumab) Injection due to temperature abuse. The affected product was distributed to Alabama, Louisiana, Mississippi, and Tennessee.
Arthrex, Inc. is recalling 9 units of 5.0 mm cannulated drill bits because the color indicator on the shaft is the incorrect color.
Daimler Vans USA is recalling 2019-2020 Sprinter vans because hydraulic power steering hoses may detach, causing fluid leaks and loss of steering assist.
Arcimoto is recalling 2019-2021 FUV, 2020-2021 Deliverator and Roadster, and 2021 Rapid Responder motorcycles. A firmware defect in the inverter may cause the vehicle's battery to shutdown without warning, increasing the risk of a crash.