The Recall Desk

State

Tennessee product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33076–33100 of 81600

  • HighNHTSA·20V110000·2020-02-25

    2019 Mercedes-Benz Sprinter Recall for Missing Steering Column Cover

    Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because the steering column casing cover may be missing, potentially allowing debris to interfere with steering.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 2500, SPRINTER 1500, SPRINTER 3500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V107000·2020-02-24

    Smart Fortwo Electric Drive Recalled for Battery Fire Risk

    Mercedes-Benz is recalling one 2019 Smart Fortwo Electric Drive because a battery weld may detach, causing sudden failure, stalling, or fire.

    Product
    SMART — SMART FORTWO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V104000·2020-02-24

    HME Recalls 2016-2020 Emergency Vehicles Due to Fuse Box Seal Defect

    HME is recalling 2016-2020 AF1, 1871, and SFO emergency vehicles because a missing O-ring seal may allow moisture into the fuse box, potentially causing overheating or malfunction.

    Product
    HME — HME 1871, AF1, SFO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V099000·2020-02-21

    2021 Ford E-350 Recalled for Rear Axle Differential Fluid Deficiency

    The 2021 Ford E-350 may have inadequate rear axle differential fluid, risking driveshaft separation and loss of drive. Ford will inspect and adjust or replace the rear axle assembly at no cost.

    Product
    FORD — FORD F-550, E-450, E-350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V102000·2020-02-21

    CHTC HT-35 and HT-45 Buses Recalled for Non-Compliant Wheelchair Lifts

    CHTC Bus Group is recalling 2016-2018 HT-35 and HT-45 buses because their wheelchair platform lifts failed to complete the required compliance certification process.

    Product
    CHTC BUS — CHTC BUS HT-45, HT-35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E006000·2020-02-20

    Meritor Recall: Insufficient Lubrication in Specific Steer Axles

    Meritor is recalling specific steer axles due to insufficient lubrication that may damage wheel end bearings. This defect could cause the wheel to separate, leading to a loss of vehicle control.

    Product
    POWER TRAIN:AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V096000·2020-02-20

    SMC Laramie Trailers Recalled for Incorrect Tire Pressure Placard

    SMC Trailers is recalling 2019-2020 Laramie trailers because the Federal Placard lists the incorrect tire PSI, which may lead to overinflation and tire failure.

    Product
    SMC — SMC LARAMIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20076·2020-02-20

    Browning Recalls Leather Pistol Holsters Due to Firearm Safety Hazard

    Browning is recalling approximately 1,265 leather pistol holsters because the design can inadvertently change the firearm's safety switch position, posing an injury risk.

    Product
    Browning Leather Pistol Holsters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20075·2020-02-20

    Kolcraft Recalls Inclined Sleeper Accessories for Infant Suffocation Risk

    Kolcraft is recalling inclined sleeper accessories for two bassinet models to prevent infant suffocation. Consumers should stop using the accessory immediately.

    Product
    Inclined sleeper accessory included with Kolcraft Cuddle 'n Care 2-in-1 Bassinet & Incline Sleepers and Preferred Position 2-in-1 Bassinet & Incline Sleepers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1114-2020·2020-02-19

    Teleflex Medical Recalls Hudson RCI Comfort Flo Humidification Systems

    Teleflex Medical is recalling 127,293 Hudson RCI Comfort Flo Humidification Systems nationwide due to a potential risk of water flooding the column and entering the circuit during high-flow oxygen therapy.

    Product
    HUDSON RCI COMFORT FLO Humidification System, REF 2410, humidifier nebulizer kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1115-2020·2020-02-19

    Teleflex Medical Recalls Hudson RCI Comfort Flo Humidification Systems

    Teleflex Medical is recalling 95,696 Hudson RCI Comfort Flo Humidification Systems due to a potential risk of water flooding the column and entering the patient circuit during high-flow oxygen therapy.

    Product
    HUDSON RCI COMFORT FLO Humidification System With Remote Temperature Port, REF 2414, humidifier nebulizer kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1165-2020·2020-02-19

    Pacific Medical Toco M2734A Fetal Monitors Recalled for Unverified Components

    Pacific Medical Group is recalling 466 Toco M2734A fetal monitors serviced with unverified non-OEM components that may fail to detect fetal distress or cause burns.

    Product
    Toco M2734A, that may have been serviced with the following: Pacific Medical Philips Avalon Smart US/TOCO Cable Assembly, NFPHA9020; Pacific Medical Philips Avalon Smart M2734A/2735A Toco Gauge Flex, NFPHA9341
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1108-2020·2020-02-19

    Terumo Advanced Perfusion System 1 Roller Pump Recall for Shaft Failure

    Terumo is recalling 33 Advanced Perfusion System 1 Roller Pumps because the pump shafts may fail, potentially causing the pump to stop during surgery.

    Product
    Terumo Advanced Perfusion System 1 Roller Pump, 4 Inch, Catalog Number 816570 - Product Usage: is indicated for use for up to 6 hours in the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when used by a…
    Category
    Medical Device
    Distribution
    Distributed nationwide