The Recall Desk

State

Maryland product recalls

72,820 recalls have nationwide distribution and so reach Maryland. 8,217 additional recalls listed Maryland specifically in their distribution scope.

What the numbers show

Total
8,217
Critical
996
Severe
2,130
Most recent
2026-09-02

Of the 8,217 recalls naming Maryland we have scored against our rubric, 996 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,130 (26%) are Severe.

These figures cover only the 8,217 recalls whose distribution notice names Maryland specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

451–475 of 81037

  • SevereNHTSA·26V517000·2026-08-06

    Isuzu NPR HD Liftgate Deck Pin Recall

    US Truck Body is recalling 2025 Isuzu NPR HD vehicles with Waltco liftgates because deck pins may break, causing the platform to fall.

    Product
    ISUZU — ISUZU NPR HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26665·2026-08-06

    Wnttmt Baby Walkers Recalled Due to Fall and Entrapment Hazards

    Wnttmt-branded infant walkers are being recalled because they pose serious injury or death risks from falls and entrapment. These products were sold on Amazon by WURUI.BABY.

    Product
    Wnttmt Baby Walkers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26661·2026-08-06

    Attic Stairway Ladders Recalled Over Bolt Break Fall Hazard

    Louisville Ladder is recalling over 1.7 million attic stairway ladders because the bolts can break during use, creating a fall hazard. Eleven reports of bolt breakage have been received, including one injury.

    Product
    Louisville, Featherlite, Lite & Century Attic Stairway Ladders with gas struts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26648·2026-08-06

    DR Power PRO MAX30 Lawn Mowers Recalled Over Blade Control Hazard

    DR Power Equipment is recalling about 320 DR Power PRO MAX30 30-inch walk-behind power lawn mowers because the blade control system can fail, allowing the blades to keep spinning after release and posing a serious laceration hazard.

    Product
    DR Power PRO MAX30 30" Walk-Behind Power Lawn Mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V518000·2026-08-06

    Jayco Recalls 2027 Fifth Wheel Trailers Due to Auto Leveling Jack Defect

    Jayco is recalling 2027 Eagle and Heartland Sundance fifth wheel trailers because auto leveling jacks may lower during transit, increasing crash risk.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL, HEARTLAND EAGLE, SUNDANCE FIFTH WHEEL, EAGLE SLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26671·2026-08-06

    Little Rawr Silicone Pull String Teething Toys Recalled Due to Choking Hazard

    Little Rawr Silicone Pull String Teething Toys are being recalled because the silicone strings are too long and thin, posing a choking and respiratory distress risk. One report of a child experiencing respiratory distress has been received.

    Product
    Little Rawr Silicone Pull String Teething Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26672·2026-08-06

    Syera Space Astronaut LED Finger Lights Recalled Due to Battery Ingestion Risk

    Syera is recalling Space Astronaut LED Finger Lights sold on Temu because the button cell batteries can be easily accessed by children, posing a risk of serious injury or death if swallowed.

    Product
    Space Astronaut LED Finger Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V516000·2026-08-06

    International Recalls 2027 Trucks Due to Wiper Nut Loosening Risk

    International is recalling 2027 HV, HX, LT, MV, and RH trucks because a wiper nut may loosen, causing wipers to disconnect and reducing visibility.

    Product
    INTERNATIONAL — INTERNATIONAL HV, MV, RH, LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V510000·2026-08-06

    Alfa Romeo Tonale and Dodge Hornet vehicles recalled for seat belt failure

    Chrysler (FCA US, LLC) is recalling certain 2023-2026 Alfa Romeo Tonale and 2023-2025 Dodge Hornet vehicles because the rear outboard seat belts may fail to retract properly.

    Product
    ALFA ROMEO — ALFA ROMEO, DODGE TONALE, HORNET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26673·2026-08-06

    Mini Laser Pointer Keychains Recalled Due to Battery Ingestion Risk

    KC Imports and Exports is recalling Laser & LED Light Mini Laser Pointer Keychains because button cell batteries can be easily accessed by children, posing a risk of serious injury or death.

    Product
    Laser & LED Light Mini Laser Pointer Keychains
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V514000·2026-08-06

    Toyota 2024 Tacoma rear shock absorber suspension recall issued

    Toyota is recalling certain 2024 Tacoma hybrid and 2024-2025 Tacoma vehicles because their rear shock absorber assemblies may corrode and fail, potentially detaching the external oil reservoir and creating a road hazard.

    Product
    TOYOTA — TOYOTA TACOMA HYBRID, TACOMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26C005000·2026-08-06

    Evenflo Recalls Revolve180 Litemax NXT Child Seats Due to Recline Defect

    Evenflo is recalling Revolve180 Litemax NXT child seats manufactured through March 31, 2025, because a miscalibrated level indicator may cause the seat to sit too upright, increasing injury risk in a crash.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26662·2026-08-06

    Easter LED Headbands Recalled Due to Battery Ingestion Risk

    OKK Trading, Inc. is recalling three models of Easter LED Headbands because the lithium coin batteries can be easily accessed by children, posing a risk of serious injury or death.

    Product
    Easter LED Headbands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V515000·2026-08-06

    Mack Recalls 2027 Anthem and Pioneer Trucks for Marker Light Defect

    Mack Trucks is recalling 2027 Anthem and Pioneer models because center roof marker lights may fail to illuminate, reducing visibility.

    Product
    MACK — MACK ANTHEM AN (4), PIONEER PR (4)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V512000·2026-08-06

    Toyota Recalls 2026 bZ Woodland Vehicles for Electrical Short Circuit Risk

    Toyota is recalling 2026 bZ Woodland vehicles equipped with a tow converter due to an electrical short circuit risk that can disable stability control and keep brake lights on.

    Product
    TOYOTA — TOYOTA BZ WOODLAND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2735-2026·2026-08-05

    ResMed Astral 100/150 Ventilators Recalled Due to Electrolyte Leakage Risk

    ResMed is recalling Astral 100/150 ventilators because supercapacitor electrolyte leakage can damage the charger chip, trigger a fail-safe state, and interrupt ventilation therapy.

    Product
    Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory support for patients weighing more than 11lb (5kg) who require mechanical ventilation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2809-2026·2026-08-05

    Medtronic Perfusion Systems Recalls EOPA Elongated One-Piece Arterial Cannula Model 77722

    Medtronic Perfusion Systems is recalling EOPA Elongated One-Piece Arterial Cannula Model 77722 due to potential pinhole leaks in the wire-wound body during use.

    Product
    EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 77722
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2819-2026·2026-08-05

    Medical Convenience Kits Recalled Over Lidocaine Injection Supplier Quality Issues

    Windstone Medical Packaging is recalling 15 AMS medical convenience kits containing Elevaris Lidocaine HCl injection USP due to supplier quality issues reported by Elevaris Medical Devices Inc.

    Product
    AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Port Tray - RX, Part Number 008786-19
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2807-2026·2026-08-05

    Medtronic Perfusion Systems Recalls EOPA Elongated One-Piece Arterial Cannula Model 77522

    Medtronic Perfusion Systems is recalling EOPA Elongated One-Piece Arterial Cannula (Model 77522) due to potential pinhole leaks in the wire-wound body during use.

    Product
    EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 77522
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2821-2026·2026-08-05

    Bar Code Reader Wands for GEM Premier Blood Analyzers Recalled Due to Misidentification Risk

    Instrumentation Laboratory is recalling Bar Code Reader (BCR) wands used with GEM Premier 5000 and 7000 systems because they may assign patient results to the wrong patient ID.

    Product
    GEM Premier 5000 with IQM2 Model/Catalog Number: 00024019255 and GEM Premier 7000 with iQM3 Model/Catalog Number: 00000015279 Portable blood analyzer system. Affected Accessory: Bar Code Reader (BCR) Wand Part No. 00024015859
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2802-2026·2026-08-05

    Medical convenience kits recalled due to potential endotoxin level variability

    Windstone Medical Packaging, Inc. is recalling specific lots of AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits because of potential unexpected variability in endotoxin levels.

    Product
    AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Laminectomy Pack, Pack Number AMS13574A; 2) ACDF/Fusion Pack, Pack Number AMS14710B; 3) Spine Pack, Pack Number AMS14991A; 4) Spine Pack, Pack Number AMS14991B; 5) Spinal Pack, Pack Number AMS16278;
    Category
    Medical Device
    Distribution
    Distributed nationwide