The Recall Desk

State

District of Columbia product recalls

73,576 recalls have nationwide distribution and so reach DC. 2,798 additional recalls listed District of Columbia specifically in their distribution scope.

What the numbers show

Total
2,798
Critical
240
Severe
1,083
Most recent
2026-09-23

Of the 2,798 recalls naming District of Columbia we have scored against our rubric, 240 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,083 (39%) are Severe.

Which agencies issued them

These figures cover only the 2,798 recalls whose distribution notice names District of Columbia specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

176–200 of 76374

  • ModerateFDA (Devices)·Z-0118-2027·2026-10-14

    Steris HexaVue Focus Integration System Recalled for Patient Data Mismatch

    Steris is recalling 58 HexaVue Focus Integration Systems because a software issue may cause incorrect patient information to appear on printed images.

    Product
    HexaVue Focus Integration System, a single, all-in-one system that handles operating room video routing, surgical video integration, and environmental control, Software Version: 2.0.18
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0089-2027·2026-10-14

    Nihon Kohden CNS-6200 Central Nurse Station Recalled for Cybersecurity Vulnerability

    Nihon Kohden America LLC is recalling 808 CNS-6200 Series Central Nurse Stations due to a cybersecurity vulnerability that could disrupt patient monitoring.

    Product
    Product Name: Nihon Kohden CNS-6200 Series Central Nurse Station, Model/Catalog Number: CN-6201 Software Version: software versions: 01-03, 01-04, 01-05, 01-06, 02-10, 02-11, and 02-40 Product Description: The device is intended for use by medical professionals to provide…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0115-2027·2026-10-14

    Mindray cPM Series Patient Monitor Manuals Recalled for Alarm Clarification

    Mindray DS USA, Inc. is recalling cPM Series Patient Monitor operator's manuals because descriptions of physiological alarm functions may be insufficient or require clarification.

    Product
    cPM Series Patient Monitor. Operator's Manual: cPM 8/cPM 12
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0114-2027·2026-10-14

    Mindray Recalls Passport Series Patient Monitor Operator's Manuals

    Mindray DS USA, Inc. is recalling Passport Series Patient Monitor operator's manuals because descriptions of selected physiological alarm functions may be insufficient or require clarification.

    Product
    Passport Series Patient Monitor. Operator's Manuals: 8 / 12 / 12M / 17M / V
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0109-2027·2026-10-14

    Mindray ePM Series Patient Monitor Manuals Recalled for Alarm Clarification

    Mindray DS USA is recalling ePM Series Patient Monitor operator's manuals because descriptions of physiological alarm functions may be insufficient or require clarification.

    Product
    ePM Series Patient Monitor. Patient Monitor Series: ePM 10M/ePM 12M/ePM 12MA/ ePM 15M/ePM 10A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0113-2027·2026-10-14

    Mindray Recalls BeneView T5 and T8 Operator's Manuals for Alarm Clarification

    Mindray DS USA, Inc. is recalling 133 BeneView T5 and T8 operator's manuals because descriptions of physiological alarm functions may be insufficient or require clarification.

    Product
    BeneView Series. Operator's Manuals: T5 / T8
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0033-2027·2026-10-14

    Sun Pharmaceutical Recalls Tretinoin Cream Due to Impurity Failures

    Sun Pharmaceutical Industries Inc. is recalling Tretinoin Cream USP 0.05% because the product failed impurities and degradation specifications.

    Product
    TRETINOIN — TRETINOIN (TRETINOIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0112-2027·2026-10-14

    Mindray Panorama and Telemetry Monitoring System Operator's Manuals Recalled

    Mindray DS USA, Inc. is recalling Panorama and Telemetry Monitoring System operator's manuals because descriptions of selected physiological alarm functions may be insufficient or require clarification.

    Product
    Panorama and Telemetry Monitoring System. Operator's Manuals: TMS-6016/Panorama Telepack-608/TMS60 (TD60).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0110-2027·2026-10-14

    Certain Mindray patient monitor manuals need clarification of alarm functions

    Certain operator's manuals for Mindray BeneVision N1 and N-Series patient monitors contain descriptions that may be insufficient or need clarification about selected physiological alarm functions.

    Product
    BeneVision N1 and N-Series Patient Monitor. Patient Monitor: N12/N15/N17/N19/N22.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0111-2027·2026-10-14

    Mindray BeneVision Telemetry Monitor Manuals Recalled for Alarm Clarification

    Mindray DS USA, Inc. is recalling BeneVision Series Telemetry Monitor operator's manuals because descriptions of selected physiological alarm functions may be insufficient or require clarification.

    Product
    BeneVision Series Telemetry Monitor. Operator's Manuals: TM70/TM80
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0116-2027·2026-10-14

    Mindray T1 Patient Monitor Operator's Manual Recall for Alarm Descriptions

    Mindray DS USA, Inc. is recalling T1 Patient Monitor Operator's Manuals because descriptions of physiological alarm functions may be insufficient or require clarification.

    Product
    T1 Patient Monitor. Operator's Manual: T1 Patient Monitor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V672000·2026-10-13

    KZRV SportTrek Fifth Wheel Trailers Recalled for Wiring Fire Risk

    K.Z., Inc. is recalling 2026-2027 SportTrek Fifth Wheel recreational trailers because the charge line may lack circuit protection, increasing the risk of a fire.

    Product
    KZRV — KZRV SPORTTREK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V671000·2026-10-09

    Volvo Recalls EX30 and EX30CC Vehicles for Head Restraint Defect

    Volvo is recalling 2025-2026 EX30 and 2026 EX30CC vehicles because the head restraint cushion may detach during a crash, increasing injury risk.

    Product
    VOLVO — VOLVO EX30CC, EX30
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E070000·2026-10-09

    Lippert Recalls Power Seating Assemblies Due to Fuse Defect

    Lippert is recalling power seating assemblies because the power cord fuse may not provide adequate circuit protection, increasing the risk of a fire.

    Product
    ELECTRICAL SYSTEM:WIRING:FUSES AND CIRCUIT BREAKERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V666000·2026-10-09

    Altec Recalls 2026 Vehicles Missing Rearview Cameras

    Altec is recalling 2026 Service Body, Aerial Device, Digger Derrick, and AC Series Crane vehicles that may lack rearview cameras, increasing crash risk.

    Product
    ALTEC — ALTEC SERVICE BODY, DIGGER DERRICK, AERIAL DEVICE, AC SERIES CRANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·27022·2026-10-08

    Avengers Infinity Gauntlet Medals Recalled for Magnet Ingestion Risk

    The Conqueror is recalling Avengers Infinity Gauntlet Medals because high-powered magnets may detach, posing a serious injury or death risk to children.

    Product
    Avengers Infinity Gauntlet Medals
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·27019·2026-10-08

    Pacearth Recalls Swing Seats Due to Serious Injury Risk from Falling

    Pacearth Direct is recalling PACEARTH Swing Seats because components can break, posing a fall hazard. The company has received reports of falls resulting in injuries.

    Product
    PACEARTH Swing Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·27017·2026-10-08

    Decathlon Recalls Van Rysel GRVL AF Bicycles Due to Crash Hazard

    Decathlon America is recalling about 1,150 Van Rysel GRVL AF bicycles because a front lock nut can loosen, causing the wheel to dislodge and posing a crash risk.

    Product
    Van Rysel GRVL AF Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V664000·2026-10-08

    Hyundai and Genesis Recall Vehicles Due to Front Seat Fire Risk

    Hyundai Motor America is recalling 2015-2020 Genesis and G80 vehicles because front power seat motors may overheat and cause a fire.

    Product
    GENESIS — GENESIS, HYUNDAI G80, GENESIS
    Category
    Vehicle
    Distribution
    Distributed nationwide