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.
Zimmer Biomet is recalling NCB-PH plates because non-highly polished implants may adhere to the LDPE bag packaging.
Zimmer Biomet is recalling Sidus Stem-Free Shoulder Humeral Head implants because non-highly polished units may adhere to the LDPE bag.
Zimmer Biomet is recalling Coorad Morrey Total Elbow implants because non-highly polished components may adhere to the packaging bag.
Zimmer Biomet is recalling Metasul Taper Liners because non-highly polished implants may adhere to the LDPE bag. The recall covers devices manufactured prior to January 2014.
Zimmer Biomet is recalling Cable-Ready Short and Long GTR implants because non-highly polished units may adhere to the LDPE bag.
Zimmer Biomet is recalling Metasul Femoral Heads because non-highly polished implants may adhere to the LDPE bag packaging.
Biomedical Polymers is recalling Manual Diff Droppers because the metal cannula may break or fail to pierce blood specimen tubes.
Zimmer Biomet is recalling Trabecular Metal Reverse Shoulder System implants because non-highly polished components may adhere to the packaging bag.
Zimmer Biomet is recalling NCB Proximal Lateral Tibia implants because non-highly polished devices may adhere to the packaging bag.
Zimmer Biomet is recalling various knee systems because non-highly polished implants may adhere to the LDPE bag.
Zimmer Biomet is recalling BF Humeral Stems because non-highly polished implants may adhere to the LDPE bag packaging.
Zimmer Biomet is recalling 5.4 million cephalomedullary nails because non-highly polished implants may adhere to the packaging bags.
Zimmer Biomet is recalling Prox Lat Humeral Lock Plates because non-highly polished implants may adhere to the LDPE bag packaging.
Zimmer Biomet is recalling 5,459,583 Connection Screws for NCB Plates because non-highly polished implants may adhere to the LDPE bag.
Zimmer Biomet is recalling 5.4 million ankle implants because non-highly polished devices may adhere to the packaging bag.
Zimmer Biomet is recalling specific spinal plates because non-highly polished implants may adhere to the packaging bag.
Randox Laboratories is recalling 100 kits of Liquid Protein Calibrators because the assigned value for Rheumatoid Factor over-recovered against the reference material. The calibrator values have been adjusted to re-align to the reference material.
Zimmer Biomet is recalling 5.4 million hip joint replacement systems because non-highly polished implants may adhere to the LDPE bag packaging.
Zimmer Biomet is recalling 5.4 million temporary surgical devices because non-highly polished implants may adhere to the packaging bag.
Zimmer Biomet is recalling 5,459,583 periarticular femur plates because non-highly polished implants may adhere to the LDPE bag packaging.
Sato Pharmaceutical Inc. is recalling Sankaijo Botanical Laxative tablets because the sennosides content is lower than the labeled claim.
Aston Martin is recalling 2018-2019 DB11, Vantage, and DBS Superleggera vehicles because passenger air bag fasteners may not be tightened properly, increasing injury risk in a crash.
Ford is recalling 2019-2020 F-150 vehicles because a battery cable fastener may loosen, potentially causing engine stalling, loss of braking or steering assist, or fire.
Ford is recalling 2016-2017 Lincoln MKX vehicles with 3.7L engines because the battery cable harness may contact a bracket, causing a short circuit and increasing fire risk.
Matrix Headgear is recalling Alpha motorcycle helmets because the retention system may fail, allowing the helmet to separate from the head during a crash.