The Recall Desk

State

Maryland product recalls

72,913 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.

Which agencies issued them

These figures cover only the 8,218 recalls whose distribution notice names Maryland specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1951–1975 of 81131

  • ModerateFDA (Devices)·Z-2168-2026·2026-05-20

    Hologic 3DIMENSIONS MAMMOGRAPHY SYSTEM medical device recall

    Hologic is recalling certain 3DIMENSIONS MAMMOGRAPHY SYSTEM models due to internal bolts that may become loose, missing, or broken over time. The FDA classified this as a Class II recall.

    Product
    3DIMENSIONS MAMMOGRAPHY SYSTEM; Model Numbers: 3DM-SYS-INTL2D, 3DM-SYS-INTL2D-MOB, 3DM-SYS-INTL2D-NS, 3DM-SYS-INTL3D, 3DM-SYS-INTL3D-MOB, 3DM-SYS-INTL3D-NS, 3DM-SYS-STD, 3DM-SYS-STD-MOB, 3DM-SYS-STD-NS.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2195-2026·2026-05-20

    Daig Livewire Steerable Electrophysiology Catheter Incomplete Seals Recall

    Stryker Sustainability Solutions is recalling 206 units of Daig Livewire Steerable reprocessed electrophysiology catheters due to incomplete seals on sterile product. The catheters were distributed nationwide and in Israel and Canada.

    Product
    Daig Livewire Steerable, Product Number 401915; REPROCESSED ELECTROPHYSIOLOGY CATHETER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2155-2026·2026-05-20

    Revolution Apex Select CT systems subject to software security vulnerability recall

    GE HealthCare is recalling Revolution Apex Select and related CT systems due to a security vulnerability in the AW Server software deployed via Edison Health Link-based CT Smart Subscription.

    Product
    Revolution Apex Select, X-ray Computed Tomography, Model Number 5590000-27
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2173-2026·2026-05-20

    Codman CerebroFlo EVD Catheter recalled for out-of-specification endotoxin

    Integra LifeSciences is recalling Codman CerebroFlo EVD Catheters (Lot 45322) because endotoxin levels did not meet acceptance criteria. The product was distributed nationwide.

    Product
    Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.550.501. The CerebroFlo EVD Catheter is a 3.3 mm diameter (10 Fr.), 35 cm long polyurethane catheter for diverting cerebrospinal fluid (CSF) from the ventricles of the brain through a series
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0777-2026·2026-05-20

    Swad orange masala candy contains undeclared FD&C Yellow 6

    Swad Orange Flavored Masala Candy is being recalled because it contains undeclared FD&C Yellow 6. The action covers 205 cases.

    Product
    Swad Orange Flavored Masala Candy
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-2134-2026·2026-05-20

    DonJoy IceMan Classic Cube cold therapy unit connector defect recall

    DJO, LLC is recalling DONJOY ICEMAN CLASSIC CUBE cold therapy units due to broken connectors that may interrupt prescribed cold therapy. Approximately 596 units were distributed nationwide and in Canada.

    Product
    Brand Name: DONJOY Product Name: ICEMAN CLASSIC CUBE Model/Catalog Number: 11-0494 Software Version: no Product Description: 11-0494 - ICEMAN CLASSIC CUBE The IceMan CLASSIC3¿ cold therapy unit helps reduce pain and swelling, speeding up rehabilitation. The IceMan¿ helps pro
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2137-2026·2026-05-20

    DonJoy IceMan cold therapy unit recall due to broken connector

    DJO, LLC is recalling the DonJoy IceMan CLASSIC3 cold therapy unit (model 11-9099) due to a broken connector that may interrupt prescribed cold therapy. The affected unit is lot 110525, distributed across the US and Canada.

    Product
    Brand Name: DONJOY Product Name: ICEMAN, W/COLDPAD, NS, RH Model/Catalog Number: 11-9099 Software Version: No Product Description: 11-9099 - ICEMAN, W/COLDPAD, NS, RH The IceMan CLASSIC3¿ cold therapy unit helps reduce pain and swelling, speeding up rehabilitation. The IceMa
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2154-2026·2026-05-20

    Revolution Apex X-ray CT System Security Vulnerability Recall

    GE HealthCare is recalling Revolution Apex, Revolution Ascend, and Revolution CT systems due to a potential security vulnerability in the AW Server deployed via Edison Health Link-based CT Smart Subscription. The vulnerability may impact system security.

    Product
    Revolution Apex, X-ray Computed Tomography, Model Number 5590000-20
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0778-2026·2026-05-20

    Swad mango masala candy contains undeclared Blue 1 coloring

    Swad Mango Flavored Masala Candy is being recalled because it contains undeclared Blue 1. The action covers 205 cases.

    Product
    Swad Mango Flavored Masala Candy
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-2152-2026·2026-05-20

    Revolution Apex Plus CT System Security Vulnerability Recall

    GE HealthCare is recalling Revolution Apex Plus X-ray CT systems due to a potential security vulnerability in the AW Server deployed via Edison Health Link. Eleven units are affected worldwide.

    Product
    Revolution Apex Plus, X-ray Computed Tomography, Model Number 5590000-25
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2172-2026·2026-05-20

    Edwards EVOQUE Tricuspid Delivery System Labeling Update for Valve Functionality

    Edwards Lifesciences is updating labeling for the Edwards EVOQUE tricuspid delivery system (REF 9850TDS) to provide a warning if valve replacement delivery system functionality becomes compromised.

    Product
    Edwards EVOQUE tricuspid delivery system REF:9850TDS Sterile EO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2151-2026·2026-05-20

    Revolution Apex Elite X-ray CT System Security Vulnerability Recall

    GE HealthCare is recalling certain Revolution Apex Elite X-ray computed tomography systems due to a potential security vulnerability in the AW Server deployed via Edison Health Link. The vulnerability may affect data security in CT Smart Subscription systems.

    Product
    Revolution Apex Elite, X-ray Computed Tomography, Model Number 5590000-23
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2153-2026·2026-05-20

    Revolution CT ES X-ray Computed Tomography System Security Vulnerability Recall

    GE Medical Systems is recalling Revolution CT ES and related CT systems due to a potential security vulnerability in the AW Server deployed via Edison Health Link based CT Smart Subscription. The vulnerability may affect system security.

    Product
    Revolution CT ES, X-ray Computed Tomography, Model Number 5590000-15
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V314000·2026-05-18

    Hyundai Ioniq rear suspension fasteners may loosen and detach

    Hyundai is recalling certain 2025 Ioniq 5 and 2026 Ioniq 9 vehicles because the rear suspension fasteners may loosen and detach, which can cause a loss of vehicle control.

    Product
    HYUNDAI — HYUNDAI IONIQ 5, IONIQ 9
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V316000·2026-05-18

    2025–2026 Hyundai Tucson and Santa Cruz Front Camera Software Issue

    Hyundai is recalling certain 2025 and 2026 Tucson, Tucson Hybrid, Tucson PHEV, and Santa Cruz vehicles due to front camera software that may cause the forward collision avoidance system to activate prematurely and unexpectedly apply the brakes, increasing crash risk.

    Product
    HYUNDAI — HYUNDAI TUCSON, TUCSON PLUG-IN HYBRID, SANTA CRUZ, TUCSON HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V313000·2026-05-18

    2026 Keystone Alpine recreational trailers recalled for loose shock bolts

    Keystone RV Company is recalling certain 2024–2026 recreational trailers because shock bolts may have been incorrectly tightened, which could cause loss of vehicle stability and increase crash risk.

    Product
    KEYSTONE — KEYSTONE ALPINE, COUGAR, MONTANA, WALKABOUT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V315000·2026-05-18

    Tesla 2025-2026 Model Y Vehicles Missing Certification Label

    Tesla is recalling certain 2025 and 2026 Model Y vehicles because the certification label may not have been installed. Missing weight information on the label could lead to vehicle overloading and increase crash risk.

    Product
    TESLA — TESLA MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V310000·2026-05-15

    Altec Recalls Aerial Devices Due to Emergency Stop Failure

    Altec is recalling specific aerial device vehicles because the ground-level emergency stop may fail to halt hydraulic functions in ePTO mode, increasing injury risk.

    Product
    ALTEC — ALTEC AT SERIES, TA SERIES AERIAL DEVICE, AN SERIES AERIAL DEVICE, L SERIES AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V307000·2026-05-14

    Hyundai Recalls Elantra Vehicles Due to Air Bag Inflator Rupture Risk

    Hyundai is recalling 2015-2016 Elantra and 2016 Elantra GT vehicles because the driver's air bag inflator may rupture during deployment, posing a risk of injury from metal fragments.

    Product
    HYUNDAI — HYUNDAI ELANTRA GT, ELANTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26485·2026-05-14

    Agio Menlo Woven Patio Swings Recalled Due to Fall Hazard Risk

    World Bright International Limited recalls Agio Menlo Woven Patio Swings (Model 1934256) sold at Costco because the swing seat can detach during use, risking serious injury or death. Eight injuries have been reported.

    Product
    Agio Menlo Woven Patio Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26493·2026-05-14

    Cosyland Children's Tower Stools Recalled for Entrapment and Fall Hazards

    Cosyland Children's Tower Stools can collapse, tip over, or trap a child's torso through front and back openings, posing risks of serious injury and death. The firm is aware of 25 reports of stability issues and falls, with eight injuries including a fractured arm.

    Product
    Cosyland Children's Tower Stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26481·2026-05-14

    Tiyol Pull String Teething Toys Recalled for Choking Hazard Risk

    Tiyol Pull String Teething Toys sold on Amazon are recalled due to oversized silicone strings that can lodge in the throat, posing a choking hazard. CPSC is aware of 11 choking incidents.

    Product
    Tiyol Pull String Teething Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide