The Recall Desk

State

Tennessee product recalls

72,986 recalls have nationwide distribution and so reach Tennessee. 7,821 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total
7,821
Critical
1,317
Severe
1,653
Most recent
2026-09-16

Of the 7,821 recalls naming Tennessee we have scored against our rubric, 1,317 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,653 (21%) are Severe.

These figures cover only the 7,821 recalls whose distribution notice names Tennessee specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6901–6925 of 80807

  • ModerateFDA (Devices)·Z-1745-2025·2025-05-21

    Contour Gold Eyelid Weight implants recalled for mislabeling

    Meddev Corp is recalling Contour Gold Eyelid Weight implants (Model LL3012) due to mislabeling. Thirty-four weights distributed nationwide are affected.

    Product
    Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog Number: LL3012 Product Description: Contour Gold Eyelid Weight, 1.2 gm MedDev Contour and ThinProfile Eyelid Weight Implants are designed for the gravity-assisted treatment of protracted permanent
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0418-2025·2025-05-21

    La Roche-Posay Effaclar Acne Treatment Kits Recalled Nationwide

    L'Oreal USA is recalling La Roche-Posay Effaclar 3-Step Acne Routine Kits nationwide due to trace levels of benzene detected in one lot. As a precaution, all Effaclar Duo Dual Action Acne Treatment lots are included in the recall.

    Product
    La Roche-Posay Laboratoire Dermatologique Effaclar Dermatological Acne System, 3 Step Acne Routine Kit, Medicated Gel Cleanser 3.4 fl. oz. (100 mL) Tube, Clarifying Solution 3.4 fl. oz. (100 mL) Tube, Dual Action Acne Treatment 0.7 fl. oz. (20 mL: UPC 883140035275) Tube, (benzoyl
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1764-2025·2025-05-21

    CMS8000 Patient Monitor Has Nine Cybersecurity Vulnerabilities

    The CMS8000 Patient Monitor manufactured by Contec Medical Systems Co., Ltd. has nine identified cybersecurity vulnerabilities. The FDA is issuing this Class II recall affecting approximately 7,773 units distributed nationwide.

    Product
    CMS8000 Patient Monitor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1744-2025·2025-05-21

    Contour Gold Eyelid Weight implants recalled for mislabeling

    Meddev Corp is recalling Contour Gold Eyelid Weight implants (Model LL3010, 1.0 gm) due to mislabeling. The recall affects 34 units distributed nationwide across 17 states.

    Product
    Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog Number: LL3010 Product Description: Contour Gold Eyelid Weight, 1.0 gm MedDev Contour and ThinProfile Eyelid Weight Implants are designed for the gravity-assisted treatment of protracted permanent
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1784-2025·2025-05-21

    Beckman Coulter DxC 500 AU Chemistry Analyzer Software Calibration Error

    Beckman Coulter is recalling the DxC 500 AU Clinical Chemistry Analyzer due to a software error that prevents the analyzer from completing calibration orders under certain conditions, which can delay test result reporting.

    Product
    DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065. The Beckman Coulter DxC 500 AU Clinical Chemistry Analyzer is an automated chemistry analyzer that measures analytes in samples, in combination with appropriat
    Category
    Medical Device
    Distribution
    17 states
  • ModerateFDA (Devices)·Z-1747-2025·2025-05-21

    FoundationOne Companion Diagnostic reports clinically relevant variants requiring amendment

    Foundation Medicine is recalling four FoundationOne Companion Diagnostic (F1CDx) test reports sent to customers that contained clinically relevant variants requiring amendment, including one with an incorrect negative companion diagnostic claim.

    Product
    FoundationOne Companion Diagnostic (F1CDx)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V328000·2025-05-20

    Orange EV Recalls Electric Trucks Due to Obstructed Backup Lights

    Orange EV is recalling specific electric trucks because a pintle hook blocks the backup lights, reducing visibility and increasing crash risk.

    Product
    ORANGE EV — ORANGE EV E-TRIEVER, HUSK-E, T-SERIES ELECTRIC TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V327000·2025-05-20

    Braun Recalls Demers Ambulances Due to Unsecured Cushion Equipment Storage

    Braun Industries is recalling specific Demers ambulance models because improperly installed cushion equipment storage may allow items to detach during transit, increasing injury risk.

    Product
    DEMERS — DEMERS, DEMERS AMBULANCES TSE, TXE, MX164E, MXP150E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V319000·2025-05-16

    Isuzu Recalls 2025 NRR EV Due to Electrical Overheating Risk

    Isuzu is recalling 2025 NRR EV vehicles because a gap in the electrical system may cause overheating and loss of drive power, increasing crash risk.

    Product
    ISUZU — ISUZU NRR EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·25285·2025-05-15

    Chill Pill Magnetic Haptic Fidget Toys recalled due to ingestion hazard

    FidgetThings is recalling Chill Pill Magnetic Haptic Fidget Toys Red Bumpy because they violate federal magnet regulations and pose a risk of serious injury or death if swallowed by children.

    Product
    Chill Pill Magnetic Haptic Fidget Toys Red Bumpy
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25279·2025-05-15

    NICREW Submersible RGB LED Lights Recalled for Coin Battery Ingestion Hazard

    NICREW 15" Submersible RGB LED Lights with remote controls are recalled because the remote's lithium coin battery can be easily accessed by children, creating a serious ingestion hazard that can cause internal burns and death.

    Product
    NICREW 15" Submersible RGB LED Lights with remote controls
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25286·2025-05-15

    Child Safety Gates Recalled for Entrapment and Fall Hazards

    Multiple child safety gates sold on Amazon.com violate federal safety regulations, posing risk of serious injury or death from entrapment and falls. Consumers should stop using the gates immediately and contact the seller for disposal and refund.

    Product
    Child Safety Gates
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25280·2025-05-15

    Digital Wall Clocks recalled for ingestion hazard from coin battery

    Leon Rading Co. Ltd. is recalling digital wall clocks (model PH-05) sold on Amazon because the remote control contains a lithium coin battery that children can easily access and swallow, risking serious internal injury or death.

    Product
    Digital Wall Clocks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V323000·2025-05-15

    School bus parking brake can release while wheelchair lift is deployed

    International is recalling certain 2025-2026 IC Bus CESB school buses because the parking brake can be released while the wheelchair platform lift is deployed, failing FMVSS 403.

    Product
    IC BUS — IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25278·2025-05-15

    Boyro Baby Convertible High Chairs Recalled for Fall and Entrapment Hazards

    Boyro Baby Convertible High Chairs sold on Amazon.com pose a risk of serious injury or death from falls and entrapment. The restraint system is not properly attached and can fail, and the opening between seat and tray is large enough for a child to become trapped.

    Product
    Boyro Baby Convertible High Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V269000·2025-05-15

    Volkswagen ID. Buzz third-row bench seats three but has two belts

    Volkswagen is recalling certain 2025 ID. Buzz vehicles because the third-row bench is wide enough for three passengers but is designed for two and has only two seat belts, failing FMVSS 208.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID. BUZZ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25282·2025-05-15

    LivingCaring Adult Portable Bed Rails recalled for entrapment and asphyxiation risk

    LivingCaring Adult Portable Bed Rails pose a serious risk of entrapment and asphyxiation due to violations of federal safety regulations. About 280 units sold online May 2024–March 2025 are affected; consumers should stop using them immediately.

    Product
    LivingCaring Adult Portable Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25281·2025-05-15

    PlayTab Rollers Tile Toys Recalled for Magnet Ingestion Hazard

    Fat Brain Toy Co. is recalling PlayTab Rollers Tile Toys because they contain magnets that can become loose and be swallowed by children, posing a risk of serious injury or death.

    Product
    PlayTab Rollers Tile Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V321000·2025-05-15

    Keystone Recalls Travel Trailers With Detachable Step Bracket Defect

    Keystone RV Company is recalling specific 2024-2025 travel trailers because step mounting bolts may loosen, allowing steps to detach and increase injury risk.

    Product
    KEYSTONE — KEYSTONE RESIDENCE, RETREAT, SPRINGDALE, VOLTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25283·2025-05-15

    Off-Road Motorcycles Recalled Due to Brake Caliper Crack Hazard

    KTM is recalling about 19,310 GASGAS and Husqvarna off-road motorcycles from model years 2022–2025 because the front brake caliper can crack, reducing braking effectiveness and creating a crash risk. No injuries have been reported.

    Product
    GASGAS and Husqvarna Off-Road Motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25287·2025-05-15

    Children's Mini Danica Loungewear Sets Recalled for Burn Hazard Risk

    BuddyLove is recalling about 940 children's Mini Danica loungewear sets (sizes 3–12) sold from October 2023 through July 2024 because they violate federal flammability standards for children's sleepwear, posing a burn hazard and risk of serious injury or death.

    Product
    Children's Mini Danica Loungewear Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25284·2025-05-15

    Polaris Ranger XP 1000 NorthStar Recreational Off-Road Vehicles Seat Belt Fastener Recall

    Polaris is recalling about 640 Model Year 2023–2025 Ranger XP 1000 NorthStar and NorthStar Crew off-road vehicles because seat belt anchor fasteners may not be properly tightened, risking seat belt separation in a crash and potential ejection of riders.

    Product
    Model Year 2023-2025 Ranger XP 1000 NorthStar and Ranger XP 1000 NorthStar Crew Recreational Off-Road Vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V322000·2025-05-15

    Toyota Tundra reverse lights can fail from moisture in the assembly

    Toyota is recalling certain 2022-2025 Tundra and Tundra Hybrid vehicles because moisture may enter the reverse light assemblies and cause the lights to fail.

    Product
    TOYOTA — TOYOTA TUNDRA HYBRID, TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1662-2025·2025-05-14

    CADD Solis HSPCA Pump wireless connection alarm interruption recall

    Smiths Medical is recalling CADD Solis HSPCA Pumps with wireless connection modules that may experience intermittent connection alarms, interrupting active infusions and risking serious patient injury or death.

    Product
    CADD Solis HSPCA Pump ***Updated 5/27/26*** Scope updated to apply specifically to customers using the wireless system. Affected products associated with the change in scope: PUMP KIT, CADD SOLIS HPCA, MDL 2110, V4.3, ENGLISH, 1/EA 21-2111-0403-51 PUMP KIT, CADD SOLIS HPCA, MDL
    Category
    Medical Device
    Distribution
    Distributed nationwide