The Recall Desk

State

Tennessee product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1551–1575 of 81596

  • ModerateFDA (Drugs)·D-0729-2026·2026-07-29

    FDA Recalls Xylocaine Injections Due to Hair Contamination

    FDA is recalling Xylocaine (lidocaine HCl) injections due to the presence of particulate matter, specifically hair found in the product.

    Product
    XYLOCAINE — XYLOCAINE (LIDOCAINE HYDROCHLORIDE,EPINEPHRINE BITARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2675-2026·2026-07-29

    BOSS Xe Family Aiming Devices Recalled for Software Safety Enhancement

    Wilcox Industries Corp. is recalling BOSS Xe family aiming devices to implement a software enhancement designed to increase safety.

    Product
    The intended use is to be paired with a weapon for aiming purposes.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0712-2026·2026-07-29

    FDA Recalls Amlodipine and Olmesartan Tablets Over Failed Dissolution Test

    Ascend Laboratories is recalling 6,192 bottles of Amlodipine and Olmesartan Medoxomil tablets nationwide due to failed dissolution specifications and Olmesartan content below specifications.

    Product
    AMLODIPINE AND OLMESARTAN MEDOXOMIL — AMLODIPINE AND OLMESARTAN MEDOXOMIL (AMLODIPINE AND OLMESARTAN MEDOXOMIL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2769-2026·2026-07-29

    Silent Nite Sleep Appliance Recalled Due to Lack of FDA Clearance

    Prismatik Dentalcraft, Inc. is recalling Silent Nite Sleep Appliances because the device does not have FDA clearance.

    Product
    Brand Name: Silent Nite Product Name: Silent Nite Sleep Appliance Model/Catalog Number: SILNT Product Description: Silent Nite Sleep Appliance is a mandibular advancement device (MAD) intended to treat snoring and mild to moderate obstructive sleep apnea (OSA).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0725-2026·2026-07-29

    Glycopyrrolate Injection Recall Due to Hair Contamination

    Fresenius Kabi is recalling Glycopyrrolate Injection due to the presence of particulate matter, specifically hair found in the product.

    Product
    GLYCOPYRROLATE — GLYCOPYRROLATE (GLYCOPYRROLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2775-2026·2026-07-29

    SnapshotGLO Wound Imaging Device Recalled Due to Battery Charging Software Issue

    Kent Imaging, Inc. is recalling SnapshotGLO Wound Imaging Devices (Models KB100 and KB100AA) because software issues may prevent the device from recharging.

    Product
    SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0736-2026·2026-07-29

    Drug Recall: Dabigatran Etexilate Capsules 150 mg by Ascend Laboratories

    Ascend Laboratories is recalling 2,717 cartons of Dabigatran Etexilate Capsules, 150 mg, because stability testing found impurities above specification.

    Product
    DABIGATRAN ETEXILATE — DABIGATRAN ETEXILATE (DABIGATRAN ETEXILATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2774-2026·2026-07-29

    Embolization devices recalled due to incorrect labeling of implant dimensions

    Micro Therapeutics, Inc. is recalling Pipeline Flex Embolization Devices because the labels may incorrectly state the implant length.

    Product
    Pipeline Flex Embolization Device with Shield Technology, 3.00 mm x 20 mm 027 REF PED2-300-20. Intracranial aneurysm flow diverter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0758-2026·2026-07-29

    Supernus Recalls Trokendi XR Capsules for Failed Dissolution Specifications

    Supernus Pharmaceuticals is recalling Trokendi XR (topiramate) capsules because they failed dissolution specifications. The recall covers 15,853 bottles distributed nationwide.

    Product
    TROKENDI XR — TROKENDI XR (TOPIRAMATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0713-2026·2026-07-29

    LIDOLOG KIT Drug Recall Over Barcode Label Wrap Issue

    Asclemed USA Inc. is recalling 18 Lidolog Kits because the label wrap covers the barcode, making it hard to scan. The recall affects products distributed within the U.S. in Tennessee.

    Product
    LIDOLOG KIT — LIDOLOG KIT (LIDOCAINE, KENALOG, POVIDONE IODINE)
    Category
    Drug
    Distribution
    1 state
  • SevereNHTSA·26V488000·2026-07-28

    Newell Recalls 2025-2027 P50 Coaches Due to Air Spring Defect

    Newell Coach Corp. is recalling 2025-2027 P50 coaches because the steer axle air spring base may crack, potentially causing loss of suspension support and increasing crash risk.

    Product
    NEWELL — NEWELL P50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V487000·2026-07-28

    Ford Recalls 2023-2025 Mustang Mach E for Rear Window Trim Defect

    Ford is recalling 2023-2025 Mustang Mach E vehicles because rear side quarter window glass trim may detach, creating a road hazard and increasing crash risk.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V486000·2026-07-27

    Foretravel Recalls Realm Motorcoaches Due to Brake Light Defect

    Foretravel is recalling 2025-2027 Realm and Realm Presidential motorcoaches because exterior brake lights may stay on, increasing crash risk.

    Product
    FORETRAVEL — FORETRAVEL REALM, REALM PRESIDENTIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V484000·2026-07-27

    Jayco Recalls 2024-2026 Entegra Motorhomes Due to Brake Light Defect

    Jayco is recalling certain 2024-2026 Entegra motorhomes because exterior brake lights may stay on when brakes are not applied, increasing crash risk.

    Product
    ENTEGRA — ENTEGRA CORNERSTONE, ASPIRE, ANTHEM, REATTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V483000·2026-07-27

    Jayco Recalls 2026 Entegra Anthem Motorhomes for Incorrect Tire Label

    Jayco is recalling 2026 Entegra Anthem motorhomes because the vehicle certification label may list the wrong tire size, which could lead to installing incorrect replacement tires.

    Product
    ENTEGRA — ENTEGRA ANTHEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V481000·2026-07-24

    Mercedes-Benz Recalls Various Models Due to Driver's Door Lock Defect

    Mercedes-Benz USA, LLC is recalling certain 2020-2026 Mercedes-Benz vehicles because a faulty door lock micro-switch may cause the vehicle to roll away.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLA45, AMG GLA35, AMG CLE53 4MATIC+, AMG C43 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V480000·2026-07-24

    Yamaha Boat Trailer Recall Issued Due to Tongue Failure Risk

    Midwest Industries is recalling 2027 Yamaha boat trailers because the tongue may fail during towing, causing the trailer to detach and increasing crash risk.

    Product
    YAMAHA — YAMAHA BOAT TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V482000·2026-07-24

    Frontrunner Recalls 2025 Transit Buses Due to Wheelchair Retract Defect

    Frontrunner is recalling 2025 transit buses because wheelchair retractors may fail to lock, increasing injury risk. Owners will be notified to have parts replaced.

    Product
    FRONTRUNNER — FRONTRUNNER FRONTRUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide