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 deaths or serious injuries are reported, 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.

Filters

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

1–25 of 52

  • SevereFDA (Devices)·Z-2835-2026·2026-08-12

    Therabody Theragun G4 PRO Charger Recalled for Fire Risk

    Therabody is recalling Theragun G4 PRO chargers because they may overheat, presenting a risk of fire, smoke, or melting.

    Product
    Charger for the Therabody Theragun, G4 PRO massage device, and products which include the 4th Generation Theragun PRO charger. G4 PRO Black US - Refurb., SKU TG02428-01 G4 PRO NA, SKU G4-PRO-PKG-NA G4-PRO-PKG-US, SKU G4 PRO US G4 PRO Black US - Refurb V, SKU TG0002428
    Category
    Consumer Product
    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
  • HighFDA (Devices)·Z-1011-2026·2026-01-28

    Convertible baby gyms recalled over floor mats that can obstruct breathing

    About 500 Mikario Trading 5-in-1 convertible baby gyms are being recalled because the floor mats can obstruct an infant's breathing.

    Product
    MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed, REF MDR107002E; 2) Semi Electric Basic Homecare Bed, 4-pack,REF MDR107002E-4
    Category
    Consumer Product
    Distribution
    4 states
  • HighFDA (Devices)·Z-2052-2023·2023-07-12

    Treadmill Recalled for Drive PCB Malfunction Causing Unexpected Belt Movement

    Full Vision Inc is recalling approximately 565 TrackMaster TMX428 treadmills due to a drive circuit board malfunction that can cause the belt to unexpectedly stop, reverse, or accelerate, posing a risk of falls or injury.

    Product
    TRACKMASTER, TREADMILL TMX428 110V, MODEL NUMBER 317-07926
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2054-2023·2023-07-12

    TrackMaster Treadmill Recalled for Drive PCB Malfunction Risk

    Full Vision Inc. is recalling 39 TrackMaster treadmills with a drive PCB malfunction that can cause unexpected stopping, reversal, or acceleration.

    Product
    TRACKMASTER, TREADMILL TMX428CP 110V, MODEL NUMBER 317-07928
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1809-2022·2022-10-05

    Dynarex Wet Wipes Recalled Due to Facility Temperature Exposure

    McKesson Medical-Surgical Inc. is recalling three Dynarex wet wipe products that may have been exposed to higher temperatures at the facility before delivery, potentially reducing their effectiveness. All lots received between June and September 2021 are affected.

    Product
    a. DYNAREX Nice'n Fresh WIPE, BABY WET 6X6.75" (140/CN12CN/CS) Catalog # 1313. b. DYNAREX DynaCare WIPE, WET FLUSHABLE ADULT 9X13" (24/PK 24PK/CS) Catalog # 1322. c. DYNAREX dynacare WIPE, WET FLUSHABLE JR 5X8" (42/BX 12BX/CS) Catalog # 1324
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1535-2022·2022-08-24

    Travel Kit Toothbrush and Toothpaste Recalled Due to Improper Storage

    Family Dollar is recalling approximately 1,555 travel kit toothbrush and toothpaste pouches that were stored in non-temperature-controlled areas. Products sold between May 1 and June 10, 2022 are affected.

    Product
    TRVL KIT TOTHBRSH CAP PASTE IN POUCH 1CT, SKU 900737
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2080-2021·2021-07-28

    Multiple Brands of Cotton Pads Recalled for Mold Contamination Risk

    Medline Industries is recalling multiple brands of cotton pads and rounds due to potential mold contamination. The affected products were distributed nationwide and internationally for use in cosmetic and personal care applications.

    Product
    Cotton Rounds/Pads under the following brand names: 1. BEAUTY 360 Extra Large Premium Cotton Ovals - two textures soft and strong 100 count; 2. BEAUTY 360 Premium Cotton Rounds - two textures soft and strong 240 count; 3. BEAUTY 360 Patterned Basic Cotton Rounds - multipurpos
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1084-2021·2021-02-17

    Wahl Heated Massager Recalled Due to Fire Hazard

    Wahl Clipper Corp is recalling 161 units of the WAHL 4212 Heated Massager because the connection between the massager and heat element can overheat, posing a fire hazard.

    Product
    WAHL 4212 HEATED MASSAGER, SKU F800000004212 - Product Usage: intended to relieve minor muscle aches and pains.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1683-2020·2020-04-15

    Firefly Child Seats Recalled Due to Broken Latches

    James Leckey Design Ltd is recalling Firefly child seats because of reports of broken latches.

    Product
    Firefly Floorsitter, Firefly Splashy Bathseat, Firefly GoTo Seat - Product Usage: The Splashy Bath-Seat is a Portable bath seat for children aged 1-8, The GoTo Seat is a light-weight, portable, postural support seat for kids, aged between 1 and 8 with disabilities.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1103-2020·2020-02-19

    Fridababy SmileFrida ToothHugger Recalled Due to Potential Metal Exposure

    Fridababy LLC is recalling SmileFrida ToothHugger toothbrushes because repeated chewing may cause the plastic head to break, exposing a small internal metal piece.

    Product
    fridababy SmileFrida the TOOTHHUGGER 18+ months Triple Angle Brush Cleans All Sides at Once
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0681-2020·2020-01-08

    DeWALT and Stanley Laser Distance Measurers Recalled for Excessive Radiation

    Stanley Black & Decker is recalling specific DeWALT and Stanley laser distance measurers because they may emit laser radiation exceeding Class II safety limits.

    Product
    The products involved are DeWALT laser distance measurers, model numbers DW0165, DW0165S, DW0330S and Stanley Fatmax FMHT77506. These products were produced for DeWALT and Stanley by a contract manufacturer.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2139-2019·2019-08-14

    Sage Products Recalls Independent Care System Due to Damaged Mouthpaste Tubes

    Sage Products Inc is voluntarily recalling a lot of Independent Care System kits because the included Sodium Bicarbonate Mouthpaste tubes may be cosmetically damaged.

    Product
    Toothete Oral Care Sodium Bicarbonate Mouthpaste, Net Wt. 1/3 oz/ 9g, included in Independent Care System. The system is an oral care convenience kit which includes: an Ultra-Soft Toothbrush, 0.5 oz. tube of Mouth Moisturizer, 0.33 oz. /9g tube of Sodium Bicarbonate Mouthpaste a
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1177-2019·2019-04-24

    ProSun V3 42 Tanning Beds Recalled for Potential High UV Output

    ProSun International is recalling nine specific tanning beds due to quality control documentation discrepancies that could result in high UV output.

    Product
    ProSun V3 42 Xlc(160w)(10 minutes) tanning bed, Model 500. Labeled as the following: PROSUN V3 42 HIGH INTENSIVE (160W) PEARL WHITE (TMAX READY), PROSUN V3 42 HIGH INTENSIVE (160W) PEARL WHITE, PROSUN V3 42 HIGH INTENSIVE (160W) RED, PROSUN V3 42 HIGH INTENSIVE (160W) PEARL W
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1884-2018·2018-06-13

    Santajoy Laser Projectors Recalled for Exceeding Federal Radiation Standards

    Santajoy Ornament & Giftware Co. is recalling E-Z Illuminations laser projectors because they may emit radiation exceeding federal standards for Class IIIa products.

    Product
    Santajoy Ornament & Giftware Co., Ltd E-Z Illuminations Northern Lights E-Z Illuminations Galaxy Laser projectors that emit various colors and light patterns for entertainment and decorative purposes.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1614-2018·2018-06-13

    11-VI Incorporated Recalls Non-Certified Laser Diode Components for Firearms

    11-VI Incorporated is recalling 323,972 non-certified laser diode components used in firearm sights because they emit more than the 5 mW limit.

    Product
    11-VI Incorporated Laser diode component Non-certified laser diode component used in laser sights for firearms
    Category
    Consumer Product
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1361-2018·2018-05-02

    Crimson Trace Laser Sights Recalled for Exceeding Power Output Limits

    Crimson Trace is recalling 184,390 laser sights for firearms because some units exceeded the 5 mW power output limit.

    Product
    Crimson Trace Corporation laser sights. The Finished Products are laser sighting systems for firearms, used for personal defense and target acquisition.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2870-2017·2017-09-20

    X-Laser High-Power Laser Projectors Recalled for Safety Standard Non-Compliance

    X-Laser is recalling 830 high-power laser light show projectors because they fail to meet federal performance standards when used in auto and music modes.

    Product
    X-Laser Laser Light Show projector models Aurora, Caliente Aurora, PSX-400, Mobile Beat Max, Mobile Beat Max MKII, X-Beam, Hawk 500 High-power laser light show projector.
    Category
    Consumer Product
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2060-2017·2017-05-17

    Savaria SL-1000 Stairlift Recalled Due to Fire Hazard

    Savaria Concord Lifts is recalling SL-1000 stairlifts because a defect in the electrical controller and motor can cause a fire.

    Product
    Savaria SL-1000 Stairlift
    Category
    Consumer Product
    Distribution
    0 states
  • LowFDA (Devices)·Z-2148-2016·2016-07-20

    Breathe Right Clear Nasal Strips Recalled for Incorrect Packaging Labels

    GSK Consumer Healthcare is recalling Breathe Right Clear nasal strips because some secondary packaging cartons were incorrectly labeled for the AU/NZ market.

    Product
    Breathe Right Clear, 30 ct. carton., UPC 7-57145-00246-7 (US), UPC 9-300673-871749 (AU/NZ)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2047-2016·2016-06-29

    Ceg Enterprises Recalls Germ Terminator Toothbrush Sanitizers Due to Heat and Cord Issues

    Ceg Enterprises is recalling Germ Terminator GT100 toothbrush sanitizers due to reports of excessive heat, power cord discoloration, and suspected counterfeit UL labels.

    Product
    Germ Terminator, Toothbrush Steam Sterilization for Oral Health. Model GT100. The Germ Terminator uses steam heat to sanitize two manual toothbrushes or two toothbrush heads. Water is poured into a reservoir in the device's housing. The steam cycle is followed by a drying cyc
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2399-2015·2015-08-26

    Winco Designer Care Cliner Recalled for Non-Fire Retardant Foam

    Winco Mfg. is recalling Designer Care Cliner chairs because the foam used was not fire retardant as required.

    Product
    Winco Designer Care Cliner w/Swing Arms - with Nylon Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2391-2015·2015-08-26

    Winco XL Convalescent Recliner Recalled for Fire Safety Defect

    Winco Mfg. is recalling XL Convalescent Recliners because the foam used was not fire retardant as required.

    Product
    Winco XL Convalescent Recliner - with Steel Casters Long term patient recliner (Nursing, Rehabilitation, Geriatric Home Use, Retirement facilities)
    Category
    Consumer Product
    Distribution
    Distributed nationwide