The Recall Desk

State

Maryland product recalls

72,940 recalls have nationwide distribution and so reach Maryland. 8,218 additional recalls listed Maryland specifically in their distribution scope.

What the numbers show

Total
8,218
Critical
996
Severe
2,131
Most recent
2026-09-09

Of the 8,218 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 2,131 (26%) are Severe.

These figures cover only the 8,218 recalls whose distribution notice names Maryland specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4676–4700 of 81158

  • SevereCPSC·26070·2025-11-06

    Children's scooters recalled after 18 reports of a front wheel detaching

    About 50 three-wheeled children's scooters are being recalled after 18 reports of the left front wheel detaching during use, resulting in three injuries.

    Product
    Three-Wheeled Children's Scooter with Foot Brake
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V763000·2025-11-06

    International Recalls 2019-2020 CV Vehicles Due to Brake Harness Defect

    International is recalling 2019-2020 CV vehicles because a brake pressure switch harness may lack protective material, potentially causing a short circuit and reduced brake performance.

    Product
    INTERNATIONAL — INTERNATIONAL CV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26075·2025-11-06

    Plush alpaca toys recalled because the eyes can detach and choke

    About 64,000 Inkari plush alpaca toys are being recalled because the eyes can detach, violating the small parts ban and posing a choking hazard to children.

    Product
    Inkari Plush Alpaca Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26081·2025-11-06

    WYBITNY children's bed rails recalled over multiple entrapment openings

    About 120 WYBITNY children's portable bed rails are being recalled because a child can become entrapped in the enclosed openings and in openings beside and above the mattress.

    Product
    Children's WYBITNY Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26074·2025-11-06

    Baby swings recalled for exceeding the incline limit for infant sleep

    About 1,020 Vevor baby swings are being recalled because they were marketed for infant sleep with an incline angle greater than 10 degrees, posing a suffocation risk.

    Product
    Vevor Baby Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26079·2025-11-06

    Bioethanol fuel containers recalled for lacking required flame mitigation devices

    About 14,000 Y'all Can DIY bioethanol fireplace fuel containers are being recalled because they lack the flame mitigation devices required under the Portable Fuel Container Safety Act.

    Product
    Y'all Can DIY Liquid Bioethanol Fireplace Fuel Containers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V767000·2025-11-06

    2022-2024 Toyota Tundra and Lexus LX/GX Engine Failure Recall

    Toyota is recalling certain 2022–2024 Tundra and Lexus LX/GX vehicles with V35A engines due to potential manufacturing debris contamination that can cause engine failure and loss of drive power, increasing crash risk.

    Product
    LEXUS — LEXUS, TOYOTA LX, GX, TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26069·2025-11-06

    Aftermarket crib and play yard mattresses recalled over deadly entrapment gaps

    About 117,900 Criblike aftermarket play yard and non-full-sized crib mattresses are being recalled because they may not fit properly, posing a deadly entrapment hazard.

    Product
    Criblike aftermarket play yard and non-full sized crib mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26072·2025-11-06

    Backpack blowers recalled because the fan wheel can break apart

    About 47,800 STIHL BR 800 Magnum backpack blowers are being recalled because the fan wheel inside the blower can break apart, posing a laceration hazard.

    Product
    STIHL BR 800 Backpack Blower
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0136-2026·2025-11-05

    Chocolate nonpareils recalled over an undeclared milk allergen in bulk cases

    Weaver Nut Company is recalling 1,760 cases of semi-sweet chocolate nonpareils with white seeds over an undeclared milk allergen. The FDA has classified the recall as Class I.

    Product
    D2645 - Nonpareils, Semi-Sweet Chocolate (White Seeds), 25lb Bulk Cases Packaged into Various Size Units After distribution.
    Category
    Food
    Distribution
    14 states
  • CriticalFDA (Devices)·Z-0164-2026·2025-11-05

    InVision operating suite recalled over ice blockage in magnet venting paths

    IMRIS is recalling the InVision 3T Operating Suite because an ice blockage in the Siemens 3 Tesla Vida magnet's venting system could rupture the helium containment system during a quench.

    Product
    IMRIS Operating Suite, InVision 3T Operating Suite, containing Siemens 3 Tesla MRI Magnet, Vida
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0162-2026·2025-11-05

    MRI operating suites with Skyra magnet recalled over venting system blockage

    IMRIS is recalling the IMRIS iMRI 3T S Operating Suite because an ice blockage in the Siemens 3 Tesla Skyra magnet's venting system could rupture the helium containment system during a quench.

    Product
    IMRIS Operating Suite, iMRI 3T S, containing Siemens 3 Tesla MRI Magnet, Skyra
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0143-2026·2025-11-05

    Veggie spring rolls recalled over undeclared shrimp in retail cartons

    Tai Foong USA is recalling 1,261 cases of Fusia Asian Inspirations Veggie Spring Rolls over undeclared shrimp. The FDA has classified the recall as Class I.

    Product
    Fusia Asian Inspirations brand Veggie Spring Rolls. Net weight: 10 oz (283.5 g).) retail package identified by UPC 4099100222258. Type of packaging: Paperboard carton with inner poly bag; 12 ct corrugated master case. Responsible firm on label: ALDI Inc. Batavia, IL 60510 (U.S
    Category
    Food
    Distribution
    23 states
  • CriticalFDA (Devices)·Z-0161-2026·2025-11-05

    Neuro operating suites recalled over ice blockage in magnet venting paths

    IMRIS is recalling the Neuro III-SV iMRI and iMRX systems because an ice blockage in the Siemens 3 Tesla Verio magnet's venting system could rupture the helium containment system during a quench.

    Product
    IMRIS Operating Suite, Neuro III-SV iMRI System, iMRX System, containing Siemens 3 Tesla MRI Magnet, Verio
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0135-2026·2025-11-05

    Christmas chocolate nonpareils recalled over an undeclared milk allergen

    Weaver Nut Company is recalling 849 cases of semi-sweet chocolate nonpareils with Christmas seeds over an undeclared milk allergen. The FDA has classified the recall as Class I.

    Product
    47518 - Nonpareil, Semi-Sweet Chocolate (Christmas Seeds), 25lb Bulk Cases Packaged into Various Size Units After distribution.
    Category
    Food
    Distribution
    14 states
  • CriticalFDA (Food)·H-0138-2026·2025-11-05

    White chocolate coconut bundt cakes recalled over an undeclared wheat allergen

    Doan's Dessert And Coffee is recalling its 3 lb 12 oz White Chocolate Coconut Bundt Cake over an undeclared wheat allergen. The FDA has classified the recall as Class I.

    Product
    White Chocolate Coconut Bundt Cake - Net Weight 3 lbs 12 oz Contains: Wheat, Soy, Milk, Eggs No UPC
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0163-2026·2025-11-05

    MRI operating suites recalled over ice blockage in the magnet venting system

    IMRIS is recalling the IMRIS iMRI 3T V Operating Suite because an ice blockage in the Siemens 3 Tesla magnet's venting system could rupture the helium containment system during a quench. The FDA classified it Class I.

    Product
    IMRIS Operating Suite, IMRIS iMRI 3T V, containing Siemens 3 Tesla MRI Magnet, vIDA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0137-2026·2025-11-05

    Frozen carrot bundt cakes recalled over an undeclared wheat allergen

    Doan's Dessert And Coffee is recalling its 4 lb Carrot Bundt Cake over an undeclared wheat allergen in ready-to-eat frozen cakes. The FDA has classified the recall as Class I.

    Product
    Carrot Bundt Cake - Net Weight 4 lbs Contains: Wheat, Soy, Milk, Eggs, Tree Nuts No UPC
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E073000·2025-11-05

    Bendix Recalls EC80 Electronic Control Units Due to Electrical Noise Issues

    Bendix is recalling specific EC80 Electronic Control Units because electrical noise may cause the unit to malfunction, potentially disabling critical vehicle safety systems.

    Product
    SERVICE BRAKES, AIR:ANTILOCK:CONTROL UNIT/MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0316-2026·2025-11-05

    Soft tissue markers recalled over potential contamination with cotton fibers

    Endomagnetics is recalling 1,760 Magseed Pro 7 cm soft tissue markers because of the potential for contamination with cotton fibers.

    Product
    Magseed Pro 7 cm soft tissue marker. Model Number: MS2-17-1-07. Product Description: The Endomag Magseed Pro Magnetic Marker System is a sterile, single use device composed of a marker preloaded in a 17ga Needle Delivery System. The Endomag Magseed Pro Marker is indicated for
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0415-2026·2025-11-05

    Cardiac control material recalled over vial to vial troponin variability

    Microgenics is recalling 4,462 units of Thermo Scientific MAS Omni CARDIO control after customers reported vial-to-vial variability with high sensitivity Troponin I assays.

    Product
    Thermo scientific MAS Omni CARDIO, Liquid Assayed Integrated Cardiac Control, Model/Catalog Number: OCRD-L, OCRD-101, OCRD-202, OCRD-303, OCRD-SP, OCRD-MP, OCRD-UL; Product Description: In Vitro Diagnostic external control
    Category
    Medical Device
    Distribution
    Distributed nationwide