The Recall Desk

State

Tennessee product recalls

20,199 recalls have nationwide distribution and so reach Tennessee. 0 additional recalls listed Tennessee specifically in their distribution scope.

About recalls in Tennessee

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Tennessee consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

9726–9750 of 20199

  • ModerateFDA (Devices)·Z-1386-2024·2024-04-03

    Philips Patient Information Center Custom Ringtones Fail When Screen Locked

    Philips Patient Information Center iX running software version 4.X may not play custom ringtones when iOS screens are locked with a passcode. Approximately 257,183 units have been distributed worldwide. No injuries have been reported.

    Product
    Patient Information Center iX (PIC iX), Model Numbers 866389, 866390 (PIC iX Expand), and 866424 (PIC iX Hardware) running Software Version Number 4.X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1387-2024·2024-04-03

    CareEvent Event Management System notification failure on locked iOS devices

    The CareEvent Event Management System's Care Assist mobile application fails to play custom ringtones when iOS device screens are locked with a passcode. This may result in missed alerts or notifications.

    Product
    CareEvent Event Management System, Model Numbers 866435 and 866436 (CareEvent Upgrade), Software Version Number C.03.X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V094000·2024-04-02

    Genesis Vehicles Seat Belt Pretensioners May Explode in Crashes

    Hyundai is recalling Genesis vehicles because front seat belt pretensioners may explode during a crash, potentially projecting metal fragments at occupants. Dealers will secure the pretensioners with a cap at no charge.

    Product
    GENESIS — 2021 GENESIS GV80
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V095000·2024-04-02

    Electra Meccanica Solo G2 and G3 recalled for sudden loss of drive power

    Electra Meccanica is recalling 2019-2023 Solo vehicles due to a defect in the motor controller or battery controller that can cause sudden loss of drive power, increasing crash risk. Owners are being notified and eligible for vehicle repurchase.

    Product
    ELECTRAMECCANICA — 2019 ELECTRAMECCANICA SOLO G2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V093000·2024-04-02

    2020 Nissan Rogue Ignition Key May Collapse While Driving

    Nissan is recalling certain 2020 Rogues and Rogue Sports due to a faulty ignition key that may collapse while driving. The collapse could shut off the engine and prevent airbag deployment in a crash.

    Product
    NISSAN — 2020 NISSAN ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V114000·2024-04-02

    Proterra buses recalled for loose steering gearbox securing bolts

    Proterra is recalling 2017-2022 Catalyst and ZX5 buses because steering gearbox securing bolts may loosen due to insufficient adhesive, risking loss of steering control. Owner notifications were sent October 7, 2022.

    Product
    PROTERRA — 2022 PROTERRA CATALYST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V092000·2024-04-02

    2023 Honda CR-V Passenger Seat Back Frame Welding Defect

    Honda is recalling 2023 CR-V vehicles due to improper welding of the front passenger seat back frame, which may fail in a crash and increase injury risk.

    Product
    HONDA — 2023 HONDA CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V041000·2024-04-01

    2022 Forest River Vengeance Trailers Recalled for Incorrect Tire Pressure Labels

    Forest River is recalling certain 2022 Vengeance Fifth Wheel trailers because the tire pressure labels may display incorrect information for the front tires, which could result in under-inflated tires and increase the risk of a crash.

    Product
    FOREST RIVER — 2022 FOREST RIVER VENGEANCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V007000·2024-04-01

    Peterbilt 579 and Kenworth T680 electronic stability control software defect

    PACCAR is recalling approximately 46 Peterbilt 579 (2022-2023) and Kenworth T680 (2023) vehicles with faulty electronic stability control software that may underestimate vehicle mass, reducing crash prevention performance. Dealers will provide a free software update.

    Product
    PETERBILT — 2022 PETERBILT 579
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V040000·2024-04-01

    2021-2022 Porsche Cayenne Rear Axle Alignment Safety Recall

    Porsche is recalling 2021-2022 Cayenne vehicles due to potential rear axle misalignment following prior repairs. The defect may cause premature tire wear and increase crash risk.

    Product
    PORSCHE — 2021 PORSCHE CAYENNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V006000·2024-04-01

    2023 Triumph Speed Triple RR Radiator Fan Overheat Recall

    Triumph is recalling 2022-2023 Speed Triple RR and RS motorcycles because the radiator fan may overheat and fail, causing hot coolant to leak or spray and increasing the risk of injury and crash.

    Product
    TRIUMPH — 2023 TRIUMPH SPEED TRIPLE RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V038000·2024-04-01

    2013-2021 Grand Design recreational vehicles recalled for fire hazard

    Grand Design RVs (2013-2021) are recalled for an improperly secured 110-volt refrigerator wire that may cause electrical arcing and fire. Dealers will inspect and replace damaged wiring at no cost.

    Product
    GRAND DESIGN — 2015 GRAND DESIGN SOLITUDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·22V039000·2024-04-01

    2020-2021 Grand Design Imagine Trailers Recalled for Sharp Cabinet Handles

    Grand Design is recalling 2020-2021 Imagine travel trailers with cast aluminum cabinet handles that may have sharp edges. The sharp edges could cut or scrape occupants, and dealers will replace the handles free of charge.

    Product
    GRAND DESIGN — 2020 GRAND DESIGN IMAGINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·24175·2024-03-28

    Stateside Bead Supply Magnetic Beads Recalled for Ingestion Hazard

    Stateside Bead Supply is recalling high-powered 5mm magnetic beads sold online from November 2022 through June 2023 because they violate federal magnet safety regulations and pose an ingestion hazard. If swallowed, the magnets can lodge in the digestive system and cause serious injury or death.

    Product
    Magnetic Beads HIGH POWER 5mm
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24741·2024-03-28

    Polaris Model Year 2022–2023 Snowmobiles Recalled for Fire Hazard

    Polaris is recalling about 7,000 Model Year 2022–2023 snowmobiles equipped with PATRIOT BOOST engines because the fuel line between the fuel rails can leak, posing a fire hazard. Consumers should stop using the recalled snowmobiles and contact Polaris for a free repair.

    Product
    Model Year 2022-2023 Snowmobiles equipped with PATRIOT BOOST Engines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24742·2024-03-28

    Forias Pack and Play Mattresses Recalled for Infant Suffocation Hazard

    Forias pack and play mattresses sold on Amazon.com from May through August 2023 violate federal crib mattress safety standards and pose a suffocation hazard to infants. The product is missing required warnings and labels.

    Product
    Forias Pack and Play Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24177·2024-03-28

    BJ's Wholesale Club Recalls Berkley Jensen 72-inch Tiki Torches for Burn Hazard

    BJ's Wholesale Club is recalling about 90,000 Berkley Jensen Citronella 72-inch Tiki Torches because the torch top can break open or fall off while lit, creating a burn hazard. The company has received nine reports of the top breaking or falling, including two burn injuries.

    Product
    Berkley Jensen Citronella 72-inch Tiki Torches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24176·2024-03-28

    Purefog High Density Natural Fog Juice Liquid Recalled for Mold Risk

    Pure Brands of California is recalling Purefog High Density Natural Fog Juice Liquid because the product can expire sooner than the printed expiration date, posing a mold-exposure risk to people with compromised immune systems, damaged lungs, or mold allergies.

    Product
    Purefog High Density Natural Fog Juice Liquids
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0393-2024·2024-03-27

    FDA Recalls Unapproved Tianeptine Elixir Drug Product Nationwide

    Neptune's Fix Tianeptine Elixir, distributed nationwide by Super Chill Products, is recalled because it contains tianeptine, a substance not approved by the FDA for any medical use in the United States. Consumers should not use this product.

    Product
    Neptune's Fix, Tianeptine Elixir, Fast Acting, 0.338 fl.oz. (10 mL) bottle, Distributed By Superchill Products, 827 6th Avenue, New York, New York 10001.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1301-2024·2024-03-27

    HeartMate 3 Left Ventricular Assist System recalled for outflow graft obstruction

    The FDA is recalling the HeartMate 3 Left Ventricular Assist System due to observed outflow graft deformation that can obstruct blood flow. Patients with implanted devices should contact their healthcare provider.

    Product
    HeartMate 3 Left Ventricular Assist System (LVAS): 1. HeartMate 3 Sealed Outflow Graft with Bend Relief, Investigational Device Exemption (IDE) 2. HeartMate 3 Sealed Outflow Graft with Bend Relief, US 3. HeartMate 3 Sealed Outflow Graft with Bend Relief, OUS 4. HeartMate 3 LV
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1275-2024·2024-03-27

    Smiths Medical Pneupac Plus 300 Ventilator Cycling Malfunction

    Smiths Medical Pneupac Plus 300 ventilators may intermittently deliver continuous airflow instead of cycling breaths as designed. This malfunction affects 2,902 units distributed worldwide.

    Product
    smiths medical Pneupac paraPAC plus 300 ventilator kit without PEEP and CPAP, REF P300NUS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1274-2024·2024-03-27

    Smiths Medical Pneupac paraPAC plus 310 ventilators recalled for malfunction

    Smiths Medical is recalling paraPAC plus 310 ventilators that may malfunction by delivering continuous gas flow instead of cycling breaths. The defect affects 10,140 units distributed worldwide and prevents proper ventilation.

    Product
    smiths medical Pneupac paraPAC plus 310 ventilator kit with PEEP and CPAP, REF P310NUS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1267-2024·2024-03-27

    ARROW QuickFlash Radial Artery Catheters Recalled for Defective Component

    ARROW International is recalling 1,160,470 QuickFlash radial artery catheterization devices due to a defective guidewire handle that can cause arterial vasospasm and vessel injury.

    Product
    ARROW QuickFlash Radial Artery Catherization (wire, guide, catheter), Part Numbers: a) REF AK-04220; b) REF ASK-04220-FMH1; c) REF ASK-04220-HHC; d) REF ASK-04220-KSP; e) REF ASK-04220-PSU; f) REF ASK-04220-UCL1; g) REF ASK-04500-AH; h) REF ASK-04500-HF-S; i) R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1300-2024·2024-03-27

    FDA Recalls HeartMate II Left Ventricular Assist Systems for Graft Obstruction

    Thoratec Corp. recalls HeartMate II left ventricular assist system kits due to outflow graft deformation that could obstruct blood flow. The FDA has classified this as a Class I recall affecting 2,240 units distributed worldwide.

    Product
    HeartMate II Left Ventricular Assist System (LVAS): 1. HeartMate II Sealed Outflow Graft with Bend Relief REF 103393 2. HeartMate II LVAS Implant Kit, US REF 106015 3. HeartMate II LVAS Implant Kit, OUS REF 106016 Update (February 14, 2024) HeartMate II Left Ventricular As
    Category
    Medical Device
    Distribution
    Distributed nationwide