The Recall Desk

State

Tennessee product recalls

73,718 recalls have nationwide distribution and so reach Tennessee. 7,859 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total
7,859
Critical
1,324
Severe
1,973
Most recent
2026-10-28

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.

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.

126–150 of 81577

  • ModerateFDA (Devices)·Z-0228-2027·2026-10-28

    Boston Scientific Recalls Defective Direxion Torqueable Microcatheters

    Boston Scientific is recalling 1,292 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.

    Product
    Direxion Torqueable Microcatheter, NGMC/SINGLE/021/BERN/1RO/155; Material Number: M001195250
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0232-2027·2026-10-28

    Boston Scientific Recalls Defective Direxion Torqueable Microcatheters

    Boston Scientific is recalling 42 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.

    Product
    Direxion Torqueable Microcatheter, NGMC/SINGLE/021/SWAN/1RO/105; Material Number: M001195290
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0049-2027·2026-10-28

    Viatris Recalls Telmisartan and Amlodipine Tablets Due to Superpotent Drug Risk

    Viatris is recalling 21,620 bottles of Telmisartan and Amlodipine tablets because the Telmisartan content may exceed specifications.

    Product
    TELMISARTAN AND AMLODIPINE — TELMISARTAN AND AMLODIPINE (TELMISARTAN AND AMLODIPINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0267-2027·2026-10-28

    Medtronic InterStim Percutaneous Extensions Recalled for Incompatible Lead Selection

    Medtronic is recalling InterStim Percutaneous Extensions because selecting an incompatible lead or extension may prevent the system from working as intended, potentially delaying surgery or requiring replacement.

    Product
    InterStim Percutaneous Extensions EXT 3560022 ISTM II PERC 3560022 EXT 3560030 ISTM MICRO PERC 3560030
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0260-2027·2026-10-28

    Boston Scientific Recalls Defective Direxion Torqueable Microcatheters

    Boston Scientific is recalling 7,945 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.

    Product
    Direxion Torqueable Microcatheter, NGMC/TRANSEND/021/BERN/1RO/130; Material Number: M001195840
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0198-2027·2026-10-28

    Axonics PNE Lead Implant Kit Recall for Syringe Defects

    Axonics is recalling PNE Lead Implant Kits because included 10mL luer lock syringes may leak or break, posing a risk to users.

    Product
    PNE Lead Implant Kit REF: 1701
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0057-2027·2026-10-28

    Pritam International Recalls Brush Buddies Toothpaste Due to CGMP Deviations

    Pritam International is voluntarily recalling 320,232 tubes of Brush Buddies toothpaste nationwide due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    Brush Buddies, Crayola Silly Scents, Anticavity Fluoride Toothpaste, (sodium fluoride 0.243%) Strawberry Flavor, Net Wt. 4.0 oz (113g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-005-40, Item # 32732, UPC 8 50048 32732 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0226-2027·2026-10-28

    Boston Scientific Recalls Defective Direxion Torqueable Microcatheters

    Boston Scientific is recalling 689 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.

    Product
    Direxion Torqueable Microcatheter, NGMC/SINGLE/021/BERN/1RO/105; Material Number: M001195230
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0206-2027·2026-10-28

    Techno-Path Multichem AE Quality Control Material Recalled for Stability Issues

    Techno-Path is recalling Multichem AE quality control material because stability drift affects the Ammonia analyte, potentially delaying diagnostic results.

    Product
    Techno-Path Multichem AE Unassayed Level 2 REF: AE622X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0196-2027·2026-10-28

    Medtronic NDI Passive Spheres Recalled for Reflective Material Variation

    Medtronic is recalling NDI Passive Spheres because variation in reflective material may affect the navigation system's ability to detect and track the spheres.

    Product
    Medtronic NDI Passive Spheres REF: 8801075, Sterile EO, 5/Tray 12 Pk., Rxonly
    Category
    Medical Device
    Distribution
    52 states
  • ModerateFDA (Devices)·Z-0274-2027·2026-10-28

    Medline Medical Convenience Kits Recalled for Adhesive Removal Issues

    Medline Industries is recalling 233 medical convenience kits because they are difficult to remove from patients and leave adhesive residue on the skin.

    Product
    MEDLINE medical convenience kits labeled as: 1) FETAL SURGERY CDS-LF, Medline Kit Number/SKUCDS840214R; 2) MAJOR, Medline Kit Number/SKUDYNJ904851I; 3) ABDOMINAL TRANSPLANT, Medline Kit Number/SKUDYNJ908124B.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0225-2027·2026-10-28

    Boston Scientific Recalls Direxion Torqueable Microcatheters Due to Coating Defects

    Boston Scientific is recalling 459 units of Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.

    Product
    Direxion Torqueable Microcatheter, NGMC/SINGLE/021/STRAIGHT/1RO/155; Material Number: M001195220
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V712000·2026-10-27

    Nova Bus Recalls 2022-2024 LFS Transit Buses for Fuel Hose Defect

    Nova Bus is recalling 453 LFS and LFS Artic transit buses because fuel filter hoses may separate, causing leaks, engine stalls, and fire risks.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V710000·2026-10-27

    Heartland Recalls Fifth Wheel Trailers Due to Fire Risk

    Heartland is recalling certain fifth wheel recreational trailers because a power cord fuse may not provide adequate circuit protection, increasing the risk of a fire.

    Product
    HEARTLAND — HEARTLAND ROAD WARRIOR, GRAVITY, TORQUE, CYCLONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V707000·2026-10-23

    Gillig Recalls 2021-2026 Low Floor Buses for Fuel Hose Separation Risk

    Gillig is recalling 2021-2026 Low Floor transit buses because remote fuel filter hoses may separate, causing fuel leaks, engine stalls, and increased fire or crash risks.

    Product
    GILLIG — 2023 GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V705000·2026-10-23

    Forest River Bus Recalls Transit Buses Due to Steering Bolt Issue

    Forest River Bus is recalling certain transit buses because a steering caster bolt may come loose, potentially causing a loss of steering ability.

    Product
    FOREST RIVER BUS — FOREST RIVER BUS GLAVAL COMMUTE, GLAVAL CONCORDE II, GLAVAL ENTOURAGE, STARTRANS CANDIDATE II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V702000·2026-10-22

    Thomas Built School Buses Recalled for Weak Body Joints

    Daimler Trucks is recalling certain Thomas Built school buses because body interior joints may be too weak to protect passengers in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX2, SAF-T-LINER EFX2, SAF-T-LINER C2 JOULEY, SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·27038·2026-10-22

    CPSC Recalls CIYTI Light-Up Princess Costumes Due to Battery Ingestion Risk

    The CPSC is recalling CIYTI Light-Up Princess Costumes because accessible button batteries pose a risk of serious injury or death if swallowed. Consumers should stop using the costumes and contact the seller for a refund.

    Product
    CIYTI Light-Up Princess Costumes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·27039·2026-10-22

    VQQQ Gas Patio Heaters Recalled for Fire and Burn Hazards

    VQQQ natural gas patio heaters are being recalled because malfunctioning components can release gas, posing a risk of serious injury or death from fire and burns.

    Product
    VQQQ Natural Gas Patio Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·27041·2026-10-22

    Lithonia Lighting Recalls RSX Luminaires with Adjustable Tilt Arms

    Lithonia Lighting is recalling RSX luminaires with specific adjustable tilt arm mountings because the knuckle can fail, causing the fixture to fall and pose a risk of serious injury.

    Product
    Lithonia Lighting RSX Luminaires with AASP, AARP, AAWB, and AAWSC Adjustable Tilt Arm Mountings used for commercial outdoor lighting.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V704000·2026-10-22

    Forest River Recalls Recreational Vehicles Due to Fire Risk

    Forest River is recalling certain recreational vehicles and trailers because a power cord fuse may not provide adequate circuit protection, increasing the risk of a fire.

    Product
    FOREST RIVER — FOREST RIVER PUMA, PUMA TRACKS, PALOMINO, PALOMINO REAL-LITE CAMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide