The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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8076–8100 of 114917

  • SevereCPSC·25467·2025-09-18

    Tabletop fire pits recalled because alcohol fuel can splash and flash

    About 66,000 tabletop fire pits sold at Five Below are recalled because alcohol fuel can splash or leak during use or ignition, causing a flash fire. One report of flames escaping; no injuries.

    Product
    Tabletop Fire Pits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25468·2025-09-18

    Portable misting fans recalled after overheating while charging caused two fires

    About 22,600 IcyBreeze Buddy portable misting fans are recalled because the fan can overheat while charging and ignite. Seven overheating reports include two that resulted in fire; no injuries.

    Product
    IcyBreeze Buddy Portable Misting Fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V624000·2025-09-18

    Genesis GV60 windshield molding can detach from the vehicle

    Hyundai is recalling certain 2023-2025 Genesis GV60 electric vehicles because the stainless-steel molding at the top of the windshield assembly may detach.

    Product
    GENESIS — GENESIS GV60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V619000·2025-09-18

    GM diesel SUVs may have an incorrect fuel tank fitted

    General Motors is recalling certain Cadillac Escalade, Chevrolet Tahoe and GMC Yukon diesel vehicles because the original fuel tank may have been replaced with an incorrect tank that can leak in a rollover.

    Product
    GMC — GMC, CHEVROLET, CADILLAC YUKON, TAHOE, ESCALADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V621000·2025-09-18

    2025 Volvo VNL Truck Trailer Lights Control Module Defect

    Volvo Trucks is recalling certain 2025–2026 VNL and 2025 VNR trucks because the trailer body control module may be improperly manufactured, causing trailer lights to fail to illuminate and reducing visibility.

    Product
    VOLVO — VOLVO VNR (4), VNL (4)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V620000·2025-09-18

    2026 Volvo VNL Trucks Door Latch Cable Installation Defect Recall

    Volvo Trucks is recalling certain 2026 VNL trucks due to an incorrectly installed door latch cable that may prevent the interior door from opening, trapping occupants and increasing injury risk.

    Product
    VOLVO — VOLVO VNL (4)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25470·2025-09-18

    Portable vaporizers recalled because the lithium-ion battery can overheat

    About 5,460 Arizer Solo II portable vaporizers are recalled because the internal lithium-ion battery can overheat, produce smoke or eject material. Nine incidents have been reported; no injuries.

    Product
    Arizer Solo II portable electronic vaporizer devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25473·2025-09-18

    Baby loungers recalled for infant sleep violations and banned crib bumpers

    About 360 LXDHSTRA baby loungers are recalled because they violate the mandatory Infant Sleep Products standard and are supplied with padded crib bumpers banned by the Safe Sleep for Babies Act.

    Product
    LXDHSTRA Baby Loungers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V622000·2025-09-18

    Mack Recalls 2025-2026 Pioneer Trucks for Trailer Light Failure

    Mack Trucks is recalling 2025-2026 Pioneer vehicles because trailer lights may fail to illuminate when towing, increasing crash risk.

    Product
    MACK — MACK PIONEER PR (4)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2484-2025·2025-09-17

    Aspiration biopsy needles recalled over undetected deformed atraumatic tips

    ViziShot 2 FLEX single use aspiration needles, model NA-U403SX-4019, are recalled because of the potential for undetected, deformed atraumatic tips. The FDA classified the action as Class I. 104,508 units are affected.

    Product
    ViziShot 2FLEX. Single Use Aspiration Needle. Model Number: NA-U403SX-4019. The ViziShot 2 FLEX tissue biopsy device is made up of four main parts: a handle, a sheath, a needle, and a stylet. The sheath and needle are attached to the handle, and the stylet, which is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0572-2025·2025-09-17

    Caramel apple pecan topped brie recalled over possible Listeria contamination

    Wegmans Caramel Apple Pecan Topped Brie Cheese, small 13 oz, is recalled because it may be contaminated with Listeria monocytogenes. The FDA classified the action as Class I.

    Product
    Wegmans Caramel Apple Pecan Topped Brie Cheese -Small - 13 OZ - Clear plastic container with lid UPC: 2-77645-XXXXX-3 (X - varies by weighted price)
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·H-0570-2025·2025-09-17

    Assorted cheese flight recalled over possible Listeria monocytogenes contamination

    Wegmans Assorted Cheese Flight, sold by the pound, is recalled because it may be contaminated with Listeria monocytogenes. The FDA classified the action as Class I.

    Product
    Wegmans Assorted Cheese Flight - Varies (sold by the lb) - Black Plastic container with clear lid UPC: 2-77100-XXXXX-5 (X - varies by weighted price)
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·H-0569-2025·2025-09-17

    Camembert soft ripened cheese recalled over possible Listeria monocytogenes contamination

    Wegmans Medium Camembert Soft Ripened Cheese, 8.8 oz, is recalled because it may be contaminated with Listeria monocytogenes. The FDA classified the action as Class I.

    Product
    Wegmans Medium Camembert Soft Ripened Cheese - 8.8oz - Round wooded container; UPC: 2-77467-00000-7 , 0-77890-53515-8
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·H-0571-2025·2025-09-17

    Grilling camembert with tapenade recalled over possible Listeria monocytogenes contamination

    Wegmans Grilling Camembert with Tapenade & Roasted Tomatoes, 10 oz, is recalled because it may be contaminated with Listeria monocytogenes. The FDA classified the action as Class I.

    Product
    Wegmans Grilling Camembert with Tapenade & Roasted Tomatoes - 10 OZ - Overwrapped black and gold metal tray UPC: 2-77297-XXXXX-0 (X - varies by weighted price)
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-2549-2025·2025-09-17

    Shoulder glenoid tray kits recalled because the reamer may kick or bind

    DJO Surgical FA S Altivate Reverse Glenoid Tray kits are recalled across all lots because the reamer may kick or bind up during or immediately prior to use. 439 kits are affected.

    Product
    Brand Name: DJO SURGICAL Product Name: FA S Altivate Reverse Glenoid Tray Model/Catalog Number: None Software Version: NA Product Description: Enovis" shoulder devices are intended for treatment of patients who are candidates for shoulder arthroplasty per the Indication for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0640-2025·2025-09-17

    Mineral sunscreen recalled after SPF testing ranged from 4 to 64

    Ultra Violette Velvet Screen SPF 50 mineral sunscreen is recalled nationwide after testing produced inconsistent SPF results ranging from SPF 4 to 64. 49,275 tubes are affected.

    Product
    Ultra Violette, Velvet Screen SPF 50, Blurring Mineral Skinscreen, Zinc Oxide 22.75%, a) 15 mL, 0.5 fl. oz. per tube, NDC 84803-106-01, UPC 9355909006068, b) 50 mL, 1.7 fl. oz. per tube, NDC 84803-106-02, UPC 9355909005924, Distributed by: Grace & Fire USA Inc., 251 Little Falls…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0643-2025·2025-09-17

    AvKare chlorpromazine unit dose cartons recalled over presence of foreign substance

    Chlorpromazine Hydrochloride Tablets, USP, 50 mg, in 50-tablet unit dose cartons for AvKare, are recalled nationwide for the presence of a foreign substance. 1,512 cartons are affected.

    Product
    CHLORPROMAZINE HYDROCHLORIDE — CHLORPROMAZINE HYDROCHLORIDE (CHLORPROMAZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2556-2025·2025-09-17

    Angled punch awls recalled following failure of fusion system instruments

    TiBrid SA Angled Punch Awls in 30, 45 and 60 degree sizes are recalled following failure of fusion system instruments in the field. 15 units are affected.

    Product
    TiBrid Stand Alone Intervertebral Body Fusion Device, SA Angled Punch Awl, Sizes: 30 degree, 45 degree and 60 degree.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2547-2025·2025-09-17

    Glenoid reamer boss drills recalled because the reamer may kick or bind

    DJO Surgical Altivate Reverse Wedge Glenoid Reamer Boss Drills, 6.5 mm, are recalled across all lots because the reamer may kick or bind up during or immediately prior to use. 907 units are affected.

    Product
    Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER BOSS DRILL, 6.5mm Model/Catalog Number: 804-06-312 Product Description: Material: S.S., Non Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0637-2025·2025-09-17

    Northstar chlorpromazine 100 mg tablets recalled over N-nitroso impurity level

    Chlorpromazine Hydrochloride Tablets, USP, 100 mg, made by Zydus for Northstar Rx, are recalled nationwide because N-Nitroso Desmethyl Chlorpromazine was found above the recommended acceptable intake limit.

    Product
    CHLORPROMAZINE HYDROCHLORIDE — CHLORPROMAZINE HYDROCHLORIDE (CHLORPROMAZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide