The Recall Desk

State

Maryland product recalls

72,969 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 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6076–6100 of 81187

  • ModerateNHTSA·25V508000·2025-08-07

    2025 Nissan Frontier Daytime Running Lights Software Error

    Nissan is recalling certain 2025 Nissan Frontier vehicles due to a software logic error that may cause daytime running lights to dim unexpectedly when the idle start-stop feature cycles the engine, posing a crash risk.

    Product
    NISSAN — NISSAN FRONTIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V504000·2025-08-06

    Freightliner Business Class M2 Steering Shaft Detachment Risk

    Fontaine Modification is recalling 2022–2024 Freightliner Business Class M2 vehicles because welds on the intermediate steering shaft may crack and fail, causing loss of steering control and crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2161-2025·2025-08-06

    SafeStar 60A Plus breathing filters show a slow rising CO2 curve

    SafeStar 60A Plus bidirectional breathing system filters are being recalled following reports of a slow increase of the CO2 curve when the gas sample is taken from the filter's port. 374,700 units affected.

    Product
    SafeStar 60A Plus Filter. Bidirectionally breathing system filter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2159-2025·2025-08-06

    SafeStar 55 Plus breathing filters show a slow rising CO2 curve

    SafeStar 55 Plus bidirectional breathing system filters are being recalled following reports of a slow increase of the CO2 curve when the gas sample is taken from the filter's port. 9,885,139 units affected.

    Product
    SafeStar 55 Plus Filter. Bidirectionally breathing system filter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2160-2025·2025-08-06

    HME TwinStar HEPA Plus filters show a slow rising CO2 curve

    HME TwinStar HEPA Plus bidirectional breathing system filters are being recalled following reports of a slow increase of the CO2 curve when the gas sample is taken from the filter's port. 1,019,782 units affected.

    Product
    HME TwinStar HEPA Plus Filter. Bidirectionally breathing system filter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2158-2025·2025-08-06

    SafeStar 90 Plus breathing filters show a slow rising CO2 curve

    SafeStar 90 Plus bidirectional breathing system filters are being recalled following reports of a slow increase of the CO2 curve when the gas sample is taken from the filter's gas sampling port. 669,838 units affected.

    Product
    SafeStar 90 Plus Filter. Bidirectionally breathing system filter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2167-2025·2025-08-06

    Hamilton coaxial breathing circuits may have a crack in blue tubing

    Coaxial breathing circuit sets for HAMILTON-C1, T1 and MR1 ventilators are being recalled because the blue tubing that delivers fresh gas may be cracked, which can cause rebreathing of exhaled gases. 2,560 units affected.

    Product
    Breathing circuit set, coaxial, 1.80 m, with flow sensor and expiratory valve set, REF: 260128, used with HAMILTON-C1, HAMILTON-T1 and HAMILTON-MR1 ventilators.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V502000·2025-08-06

    2018–2025 International and IC Bus vehicles recalled for fire risk

    International Motors is recalling certain 2018–2025 International 4000 Series, MV, 1300 FBC, and IC Bus TC and CECB vehicles. A leaking brake pressure switch assembly may cause an electrical short circuit that increases fire risk while driving or parked.

    Product
    IC BUS — IC BUS, INTERNATIONAL CECB, MV, 1300FBC, 4000 SERIES 4300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V503000·2025-08-06

    IC Bus CESB School Buses Brake Pressure Switch Fire Risk Recall

    International Motors is recalling certain 2016–2024 IC Bus CESB school buses because the brake pressure switch assembly may leak brake fluid into electrical components, causing a short circuit and fire risk while driving or parked.

    Product
    IC BUS — IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2164-2025·2025-08-06

    Automated Impella Controllers may not detect a connected Impella pump

    The Automated Impella Controller, used with left heart support blood pumps, is being recalled because of a potential issue with the controller not detecting an Impella pump when it is connected. 11,031 units affected.

    Product
    Automated Impella Controller (AIC), used in left heart support blood pump, including the following: 1. Impella Controller, Packaged, AU; Product Code: 0042-0000-AU. 2. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 3. Impella Controller, Packaged, EU; Pr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2223-2025·2025-08-06

    Blood agar plates may carry Listeria monocytogenes surface contamination

    Blood Agar with 5% Sheep Blood, product number R01202, is being recalled because the products may contain surface and subsurface contamination of Listeria monocytogenes. 1,552 units affected.

    Product
    Blood Agar,5% Sheep Blood 100/PK, Product Number R01202
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2230-2025·2025-08-06

    RAPIDPoint 500 wash waste cartridge lot biases seven blood analytes

    A lot of RAPIDPoint 500 Systems Wash/Waste Cartridges is being recalled because a manufacturing error causes positive and negative bias across seven analytes. 1,477 units are affected.

    Product
    RAPIDPoint 500 Systems Wash/Waste Cartridge (4 Pack). Material Number: 10329097.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0368-2025·2025-08-06

    Reisman's cinnamon danishes recalled over undeclared wheat and soy

    Reisman's Cinnamon Danishes 3 oz are being recalled because of undeclared wheat and soy. The action covers 186,582 units across all recalled Reisman's products.

    Product
    Reisman's Cinnamon Danishes 3 oz.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·H-0377-2025·2025-08-06

    Reisman's cinnamon babka slices recalled over undeclared wheat and soy

    Reisman's Cinnamon Babka Slices 3 oz are being recalled because of undeclared wheat and soy. The action covers 186,582 units across all recalled Reisman's products.

    Product
    Reisman's Cinnamon Babka Slices 3 oz.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-2233-2025·2025-08-06

    LVP blood administration sets have potential for external cassette leaks

    LVP Blood Products Administration Sets are being recalled because of the potential for external cassette leaks. 14,280 units are affected.

    Product
    LVP Blood Products Administration Set Dual-Inlet, Low-Sorbing, Y-Site, Mesh Filter (Qty 20). Product Code: SET-0014-20.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0356-2025·2025-08-06

    Reisman's jumbo chocolate chip cookies recalled over undeclared wheat

    Reisman's Jumbo Chocolate Chip Cookies 3 oz are being recalled because of undeclared wheat. The action covers 186,582 units across all recalled Reisman's products.

    Product
    Reisman's Jumbo Chocolate Chip Cookies 3 oz.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-2224-2025·2025-08-06

    Strep Selective II Agar plates may carry Listeria monocytogenes contamination

    Strep Selective II Agar, product number R01859, is being recalled because the products may contain surface and subsurface contamination of Listeria monocytogenes. 371 units are affected.

    Product
    Strep Selective II Agar, Product Number R01859
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2206-2025·2025-08-06

    Philips Ingenia 3.0T gradient coils may act as a heat source

    Ingenia 3.0T MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 1,467 units are affected.

    Product
    Ingenia 3.0T Model Numbers (REF): (1) 781342, (2) 781377, (3) 782103;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2234-2025·2025-08-06

    LVP primary administration sets have potential for external cassette leaks

    LVP Primary Administration Sets, Single Outlet Low Sorbing, are being recalled because of the potential for external cassette leaks. 35,925 units are affected.

    Product
    LVP Primary Administration Set, Single Outlet Low Sorbing (Qty 25). Product Code: SET-0021-25.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2175-2025·2025-08-06

    Inseego dongle kit flash drives carry outdated patient monitor software

    Inseego USB8 4G Dongle Kits for the Tempus Pro Monitor are being recalled because the kit's USB flash drive contains outdated software that could revert the monitor and reintroduce a previous issue. 55 units affected.

    Product
    Inseego USB8 4G Dongle Kit, Part Number: 01-2298, which contains USB Flash Drive, Part Number: 43-2011. The kit is an accessory to the Tempus Pro Monitor, REF: 00-1007-R, 00-1024-R, 00-1026-R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2204-2025·2025-08-06

    Philips Ingenia 1.5T gradient coils may act as a heat source

    Ingenia 1.5T MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 2,279 units are affected.

    Product
    Ingenia 1.5T Model Numbers (REF): (1) 781315, (2) 718641, (3) 781396, (4) 782101, (5) 782115, (6) 782140;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2226-2025·2025-08-06

    Blood MacConkey biplates may carry Listeria monocytogenes surface contamination

    Blood/MacConkey Biplates, product number R02049, are being recalled because the products may contain surface and subsurface contamination of Listeria monocytogenes. 611 units are affected.

    Product
    Blood/MacConkey Biplate 100/PK, Product Number R02049
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2174-2025·2025-08-06

    HeartSine samaritan public access defibrillators may not deliver shocks properly

    HeartSine SAM 350P, 360P and 450P public access defibrillators are being recalled because a component manufacturing issue means the device may not function properly to deliver shocks. 190,516 units affected.

    Product
    HeartSine SAM 350P, HeartSine SAM 360P, and HeartSine SAM 450P The HeartSine samaritan¿ PAD (Public Access Defibrillator)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2214-2025·2025-08-06

    Philips MR 7700 gradient coils may act as a heat source

    MR 7700 systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 82 units are affected.

    Product
    MR 7700 Model Numbers (REF): (1) 782120, (2) 782153;
    Category
    Medical Device
    Distribution
    Distributed nationwide