The Recall Desk

State

Tennessee product recalls

73,092 recalls have nationwide distribution and so reach Tennessee. 7,851 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total
7,851
Critical
1,327
Severe
1,665
Most recent
2026-09-23

Of the 7,851 recalls naming Tennessee we have scored against our rubric, 1,327 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,665 (21%) are Severe.

These figures cover only the 7,851 recalls whose distribution notice names Tennessee specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8301–8325 of 80943

  • HighFDA (Devices)·Z-1086-2025·2025-02-12

    Philips AD7 and AD7X Patient Table Finger Entrapment Risk

    The Philips AD7 and AD7X patient tables pose a finger entrapment risk during manual repositioning. Operators and service personnel could sustain finger injuries from the gap between the longitudinal guiding rails and tabletop.

    Product
    AlluraXperFD20/15 System Code: (1) 722058
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1091-2025·2025-02-12

    Philips Azurion and Allura System Patient Tables: Finger Entrapment Risk

    Philips Azurion and Allura system patient tables may trap fingers between the guiding rails and tabletop during manual repositioning, risking finger injury to operators and service personnel.

    Product
    Azurion 7 B12 System Code: (1) 722067 (2) 722225 (3) 722235
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1080-2025·2025-02-12

    Philips recalls AlluraXper FD20 patient tables due to finger entrapment hazard

    Philips is recalling AlluraXper FD20 patient tables due to a finger entrapment hazard. During manual repositioning, fingers can get trapped between the tabletop and rails, risking injury to operators and service personnel.

    Product
    AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1077-2025·2025-02-12

    Philips AD7 and AD7X patient tables recalled due to finger entrapment risk

    Philips has recalled the AD7 and AD7X patient tables used in medical imaging systems because fingers can become entrapped between the tabletop and guiding rails during manual repositioning, potentially causing injury.

    Product
    Allura Xper FD10 Catalog (1) 722003 (2) 722010 (3)722026
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0476-2025·2025-02-12

    FGF LLC Persian Donut Recalled for Potential Listeria Contamination

    FGF LLC is recalling Persian Donut item 8201808 nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume the product and should discard it or return it to the retailer.

    Product
    item 8201808 PERSIAN DONUT 78x2.25 OZ, NET WT 9.87 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1099-2025·2025-02-12

    Belmont Medical 3-Spike Disposable Set May Leak During Use

    The Belmont Medical 3-Spike Disposable Set may leak during priming due to a crack in its female quick connector, potentially delaying warmed infusions in hospital settings.

    Product
    Belmont Medical 3-Spike Disposable Set used with the Belmont Rapid Infuser RI-2. Designed to be used in general operation in hospital or alternate care environments to provide warmed blood and fluids to any patients e10 kg requiring warmed infusion. Part Number:903-00006
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1092-2025·2025-02-12

    Philips Azurion patient tables recalled for finger entrapment hazard

    Philips is recalling Azurion 7 B20 patient tables due to a finger entrapment hazard between the tabletop and guiding rails during manual repositioning. Operators and service personnel could suffer finger injury.

    Product
    Azurion 7 B20 System Code: (1) 722068 (2) 722226 (3) 722236
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1104-2025·2025-02-12

    Integra Miltex Cryosolutions Cartridges Recalled for Premature Valve Opening

    The Integra Miltex Cryosolutions Cartridges (Model C-CA-23) are being recalled because the valve may open prematurely during assembly, causing the cartridge to empty before use. Approximately 3,352 units were distributed nationwide in the US and Canada.

    Product
    Integra Miltex Cryosolutions Cartridges 4 Pack (23.5g N2O each), Model: C-CA-23, Item: 33517;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1112-2025·2025-02-12

    Beckman Coulter Access PCT Reagent Pack Recalled for Calibration Failures

    Beckman Coulter Inc. is recalling specific lots of Access PCT Reagent Pack due to high rates of calibration failures that delay test result reporting on immunoassay systems used in healthcare and laboratory settings.

    Product
    Access PCT Reagent Pack, Catalog Number C53987, when used on Access 2 and UniCel Dxl Immunoassay Systems
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1103-2025·2025-02-12

    Nitrous Oxide Cartridges Recalled Due to Premature Valve Opening

    Integra Miltex CryoSolutions N2O cartridges are recalled because the valve may open prematurely, causing partial or complete cartridge emptying before use. Affected units were distributed nationwide and to Canada.

    Product
    Integra Miltex CryoSolutions Cartridges 10 Pack (23.5g N2O each), Model: C-CA-23, Item: 33516;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V075000·2025-02-10

    Winnebago LP tank mounting fasteners may be improperly tightened

    Winnebago is recalling certain 2025 recreational vehicles because the LP tank mounting bracket fasteners may have been improperly tightened, causing the tank to detach.

    Product
    WINNEBAGO — WINNEBAGO NAVION, MINNIE WINNIE, VITA, VIEW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V050000·2025-02-07

    Mercedes-Benz 2024 EQB 250 Electric Vehicle Battery Fire Risk

    Mercedes-Benz is recalling certain 2022–2025 EQB 250, EQB 300 4MATIC, and EQB 350 4MATIC models due to a high-voltage battery that may fail internally and cause vehicle fire while parked or driving.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQB 250+, EQB 250, EQB 350 4MATIC, EQB 300 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V070000·2025-02-07

    Storyteller Overland Recalls MODE XO Vehicles Due to Seat Mounting Defect

    Storyteller Overland is recalling 2024-2025 MODE XO vehicles because improperly welded seat floor mounting systems may loosen or detach, increasing injury risk.

    Product
    STORYTELLER OVERLAND — STORYTELLER OVERLAND MODE XO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V073000·2025-02-07

    Nikola TRE FCEV Hydrogen Tank Mounting Bolts May Cause Fuel Leak

    Nikola is recalling certain 2024–2025 TRE FCEV trucks because hydrogen tank mounting block bolts may be too long and damage the tank, creating a fire risk.

    Product
    NIKOLA — NIKOLA TRE FCEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V072000·2025-02-07

    Entegra and Jayco Recreational Vehicles Fuel Tank Support Bracket Fire Risk

    Jayco, Inc. is recalling certain 2021–2025 Entegra Launch and Jayco Terrain recreational vehicles. Grey water tank support brackets may contact and damage the fuel tank, causing a leak and fire risk.

    Product
    JAYCO — JAYCO, ENTEGRA TERRAIN, LAUNCH, LAUNCH LE, TERRAIN LE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V069000·2025-02-07

    2024–2025 Forest River Rockport work trucks E-Track system fastener failure recall

    Forest River is recalling certain 2024–2025 Rockport work trucks because incorrect fasteners may have been used to install the optional E-Track Cargo Tie Down system. The fasteners can fail, causing the system to detach from the wall and increase the risk of injury.

    Product
    FOREST RIVER — FOREST RIVER ROCKPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V074000·2025-02-07

    2022–2025 Husqvarna and GASGAS motorcycles recalled for brake caliper cracking

    KTM North America is recalling 2022–2025 Husqvarna FE 350S and FE 501S motorcycles, along with 2024–2025 GASGAS ES 350 and ES 500 models, due to front brake calipers that may crack and cause loss of front brake function.

    Product
    HUSQVARNA — HUSQVARNA, GASGAS FE 350S, ES 500, ES 350, FE 501S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V061000·2025-02-07

    Grand Design Solitude Fifth Wheel Trailers Step Tread Defect Recall

    Grand Design is recalling certain 2019–2024 Solitude fifth wheel trailers because the step tread joints may be unsupported, causing the tread to break and increasing the risk of injury.

    Product
    GRAND DESIGN — GRAND DESIGN SOLITUDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V071000·2025-02-07

    2025 Volvo EX90 Headlight Shutter Software Defect Recall

    Volvo is recalling 2025 EX90 vehicles because a software error in the low power controller may cause headlight shutters to close while driving, reducing visibility and increasing crash risk.

    Product
    VOLVO — VOLVO EX90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V067000·2025-02-07

    Zeekr Recalls One 2025 RT Vehicle for Air Bag Software Defect

    Zeekr is recalling one 2025 RT vehicle because the occupant weight sensor software may misclassify passengers or disable the air bag, increasing crash injury risk.

    Product
    ZEEKR — ZEEKR RT (OJAI)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V066000·2025-02-07

    Zeekr Recalls One 2025 RT Vehicle for Air Bag Deployment Issue

    Zeekr is recalling one 2025 RT vehicle because the C-Pillar trim may prevent the side curtain air bag from fully deploying, increasing injury risk.

    Product
    ZEEKR — ZEEKR RT (OJAI)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V068000·2025-02-07

    Zeekr Recalls One 2025 RT Vehicle for Air Bag Protection Defect

    Zeekr is recalling one 2025 RT vehicle because the seat position may prevent side curtain and passenger air bags from providing adequate neck protection during a crash.

    Product
    ZEEKR — ZEEKR RT (OJAI)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V057000·2025-02-06

    Hino Recalls 2022-2025 Trucks Due to Brake Tube Leak Risk

    Hino is recalling 2022-2025 trucks because contact with the fender can damage the front right brake tube, causing leaks that increase stopping distance.

    Product
    HINO — HINO NV7B, NV7A, NH7A, NJ7A
    Category
    Vehicle
    Distribution
    Distributed nationwide