The Recall Desk

State

Alabama product recalls

72,940 recalls have nationwide distribution and so reach Alabama. 6,341 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total
6,341
Critical
1,121
Severe
1,337
Most recent
2026-09-02

Of the 6,341 recalls naming Alabama we have scored against our rubric, 1,121 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,337 (21%) are Severe.

Which agencies issued them

These figures cover only the 6,341 recalls whose distribution notice names Alabama specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3626–3650 of 79281

  • ModerateFDA (Devices)·Z-1152-2026·2026-01-28

    M3B vital signs monitors recalled over potential cybersecurity issues

    Edan Diagnostics is recalling 354 units of its M3B Vital Signs Monitor after an FDA letter raising potential cybersecurity issues with the firm's devices.

    Product
    Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number: M3B Product Description: M3B Vital Signs Monitor is a patient monitoring device providing the patient with a continuous vital physiological monitoring of arterial blood oxygen saturation (SpO2), Pulse Rat
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1149-2026·2026-01-28

    iX series patient monitors recalled over potential cybersecurity issues

    Edan Diagnostics is recalling 379 units of its Patient Monitor models iX10, iX12 and iX15 after an FDA letter raising potential cybersecurity issues with the firm's devices.

    Product
    Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iX10, iX12, iX15 Product Description: The iX series Patient Monitors including iX10, iX12, iX15 can perform long-time continuous monitoring of multiple physiological parameters. Also, it is capable of storing
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1155-2026·2026-01-28

    Telemetry transmitters recalled over potential cybersecurity issues flagged by FDA

    Edan Diagnostics is recalling 1,457 units of its iT20 Telemetry Transmitter after an FDA letter raising potential cybersecurity issues with the firm's devices.

    Product
    Brand Name: EDAN Product Name: Telemetry Transmitter Model/Catalog Number: iT20 Product Description: iT20 collects physiological parameters by ECG cables and SpO2 sensors, then achieves data analyzing and processing. After that, data will be sent to MFM-CMS via Wi-Fi. The para
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1141-2026·2026-01-28

    Fetal and maternal monitors recalled over potential cybersecurity issues

    Edan Diagnostics is recalling 3,518 units of its Fetal & Maternal Monitor models F6, F9, F6 Express and F9 Express after an FDA letter raising potential cybersecurity issues with the firm's devices.

    Product
    Brand Name: EDAN Product Name: Fetal & Maternal Monitor Model/Catalog Number: F6, F9, F6 Express, F9 Express Product Description: The devices are bedside fetal and maternal monitors, which are used to monitor the physiological parameters of pregnant women including the fetus f
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1156-2026·2026-01-28

    Patient information centers recalled over a patch changing notification filters

    Philips North America is recalling 146 Patient Information Center iX units because a software patch modifies Mobile Event Notification filter settings without any indication to the user.

    Product
    Patient Information Center iX; Software Version Number: 4.5.0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1130-2026·2026-01-28

    Surgical laser consoles recalled over a label missing the DANGER symbol

    Leaseir Technologies is recalling two MHR Xcell surgical laser systems because the console label on the affected devices is missing the "DANGER" symbol.

    Product
    Brand Name: LEASEIR Product Name: LEASEIR MHR XCELL Model/Catalog Number: MHR 110-b Software Version: 1.5.0.0 Product Description: The Leaseir MHR Xcell is a surgical laser instrument for use in general and plastic surgery and dermatology, intended for hair removal and treatm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V044000·2026-01-26

    Grand Design fifth wheel U-bolts may loosen and shift the axle

    Grand Design is recalling certain 2021-2024 Momentum and 2022-2024 Solitude fifth wheel trailers because the U-bolt may become loose, causing the axle to move out of position.

    Product
    GRAND DESIGN — GRAND DESIGN MOMENTUM, SOLITUDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V046000·2026-01-26

    Kia vehicles recalled for instrument panel display software failure

    Kia is recalling multiple 2025–2026 models due to a software error that may cause the instrument panel display to fail, potentially hiding critical safety information like the speedometer and warning lights.

    Product
    KIA — KIA SPORTAGE PHEV, SORENTO PHEV, SPORTAGE HYBRID, SPORTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V047000·2026-01-26

    Hyundai vehicles instrument panel display software error recall

    Hyundai is recalling certain 2025–2026 Tucson Hybrid, Tucson PHEV, and other 2026 models due to a software error that may cause the instrument panel display to fail, potentially hiding critical safety information like the speedometer and warning lights.

    Product
    HYUNDAI — HYUNDAI IONIQ 5, KONA, PALISADE, PALISADE HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V045000·2026-01-26

    Keystone Recalls 2026 Coleman Travel Trailers Due to Bed Bracket Defect

    Keystone is recalling 2026 Coleman travel trailers because bed brackets may not be secured to a stud, causing the bed to fall unexpectedly and increasing injury risk.

    Product
    KEYSTONE — KEYSTONE COLEMAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V042000·2026-01-23

    Grand Design Lineage solar panel adhesive may fail allowing detachment

    Grand Design is recalling certain 2025-2026 Lineage recreational vehicles because the adhesive securing the solar panels to the roof may fail, allowing a panel to detach.

    Product
    GRAND DESIGN — GRAND DESIGN LINEAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V035000·2026-01-23

    FWMoto Recalls FLY-10 E-Bikes Due to Insufficient Brake Performance

    FWMoto is recalling 2022-2024 FLY-10 e-bikes because brake pads may provide insufficient braking performance, increasing the risk of a crash.

    Product
    FWMOTO — FWMOTO, FLY E-BIKE FLY-10
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V037000·2026-01-23

    Polestar 3 rear seat backrest striker brackets may be loose

    Polestar is recalling certain 2025 Polestar 3 vehicles because the striker brackets that secure the rear seat backrest may be loose. This fails FMVSS 207.

    Product
    POLESTAR — POLESTAR POLESTAR 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V040000·2026-01-23

    Forest River Bus Recalls 2026 Collins Buses for Body Panel Adhesive Defect

    Forest River Bus is recalling 2026 Collins Bus transit buses because body panel adhesive may be applied incorrectly, causing panels to separate and reducing structural integrity.

    Product
    FOREST RIVER BUS — FOREST RIVER BUS COLLINS BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V038000·2026-01-23

    Toyota Tundra rearview camera image may not display when reversing

    Toyota is recalling certain 2024-2025 Tundra and Tundra Hybrid vehicles with a Panoramic View Monitor because the rearview camera image may not display when the vehicle is placed in reverse.

    Product
    TOYOTA — TOYOTA TUNDRA, TUNDRA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V043000·2026-01-23

    2026 Brinkley RV Model Z Trailers Recalled for Fire Risk

    Brinkley RV is recalling certain 2026 Model Z trailers because shore power inlet lugs may be improperly tightened, causing wires to loosen, overheat, and create a fire hazard.

    Product
    BRINKLEY RV — BRINKLEY RV MODEL Z
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V039000·2026-01-23

    Forest River Recalls 2026 Trailers Due to Wiring Fire Risk

    Forest River is recalling 2026 Cherokee, Campsite Reserve, and Cascade trailers because incorrect wiring lacks over-current protection, increasing fire risk.

    Product
    FOREST RIVER — FOREST RIVER CASCADE, CAMPSITE RESERVE, CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·26215·2026-01-22

    Semi electric homecare beds recalled over hand pendants that may overheat

    Medline is recalling 373,392 units of the Semi Electric Basic Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.

    Product
    Mikario Trading 5-in-1 Convertible Baby Gyms
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·26204·2026-01-22

    Pull string teething toys recalled over silicone strings that can lodge

    About 6,800 Yetonamr Pull String Teething Toys are being recalled because the silicone strings can reach the back of the throat and become lodged. CPSC is aware of 32 choking incidents.

    Product
    Yetonamr Pull String Teething Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V031000·2026-01-22

    Chevrolet Blazer EV parking brake may activate unintentionally or fail

    GM is recalling certain 2024-2025 Chevrolet Blazer EV vehicles that may have been repaired incorrectly under recall 25V433, because the rear parking brake wiring harness may become damaged or corroded.

    Product
    CHEVROLET — CHEVROLET BLAZER EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26207·2026-01-22

    Fidget magnet ball toys recalled over loose high-powered magnets

    About 9,300 Based Online Fidget Magnet Ball Toy Sets are being recalled because they contain magnets that can be swallowed by children. CPSC reports no injuries or incidents.

    Product
    Based Online Fidget Magnet Ball Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide