The Recall Desk

State

Colorado product recalls

72,966 recalls have nationwide distribution and so reach Colorado. 6,941 additional recalls listed Colorado specifically in their distribution scope.

What the numbers show

Total
6,941
Critical
1,218
Severe
1,507
Most recent
2026-09-09

Of the 6,941 recalls naming Colorado we have scored against our rubric, 1,218 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,507 (22%) are Severe.

These figures cover only the 6,941 recalls whose distribution notice names Colorado specifically. The 72,966 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5226–5250 of 79907

  • HighNHTSA·25E067000·2025-10-10

    Ford Recalls Engine Block Heaters Due to Fire Risk

    Ford is recalling specific engine block heaters that may crack and leak coolant, causing a short circuit and increasing fire risk.

    Product
    EQUIPMENT:ELECTRICAL:ENGINE BLOCK HEATER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E065000·2025-10-09

    Chrysler Recalls Mopar Gear Shift Control Cables Due to Park Function Loss

    Chrysler is recalling specific Mopar Gear Shift Control Cables that may detach from the transmission, preventing the vehicle from shifting into park and increasing the risk of a crash.

    Product
    POWER TRAIN:AUTOMATIC TRANSMISSION:LEVER AND LINKAGE:FLOOR SHIFT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26008·2025-10-09

    Portable waist fans recalled after four reports of melting or fire

    About 48,000 Living Glow five-in-one portable waist fans are being recalled because the lithium-ion batteries can overheat while charging; four fans have melted or caught fire.

    Product
    Living Glow portable waist fan
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26007·2025-10-09

    Electric pressure cookers recalled after eight reports of severe burn injuries

    About 46,660 Ambiano electric pressure cookers sold at ALDI are being recalled because the lid can be opened before pressure is released; 11 incidents include eight severe burn injuries.

    Product
    Ambiano Electric Pressure Cookers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V677000·2025-10-09

    Braun Ambulances Recall 2023-2026 Models Due to Cruise Control Defect

    Braun Industries is recalling 2023-2026 ambulances because a damaged brake pedal switch may prevent cruise control from disengaging, increasing crash risk.

    Product
    BRAUN AMBULANCES — BRAUN AMBULANCES LIBERTY TYPE I, EXPRESS PLUS TYPE I, CHIEF XL TYPE I, SELECT CHIEF XL I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V680000·2025-10-09

    Genesis Supreme Recalls One Fifth Wheel Trailer Due to Fire Risk

    Genesis Supreme RV is recalling one 2024 Supreme 28IKS fifth wheel trailer because the air conditioner soft start device may overheat and cause a fire.

    Product
    GENESIS SUPREME — GENESIS SUPREME FIFTH WHEEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V676000·2025-10-09

    Nissan and Chevrolet Vans Recalled for Fuel Pump Fuse Short Circuit Risk

    Nissan is recalling 2013-2021 NV200 and 2015-2018 Chevrolet City Express vans because a misrouted sensor harness may damage wires, causing a short circuit that could stall the engine.

    Product
    NISSAN — NISSAN, CHEVROLET NV200, CITY EXPRESS, CHEVEROLET SS, NV200 TAXI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2659-2025·2025-10-08

    MAGNETOM Prisma MRI systems recalled over helium venting ice blockage

    Siemens is recalling 101 MAGNETOM Prisma MRI systems because an ice blockage in the magnet venting system could prevent helium escaping during a quench.

    Product
    MAGNETOM Prisma. Model Number: 10849582.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2612-2025·2025-10-08

    Reprocessed electrophysiology catheters recalled over residual particulates on patient surfaces

    Medline is recalling 7,913 reprocessed Inquiry Steerable Diagnostic Catheters because specific lots may carry small residual particulates on patient-contacting surfaces.

    Product
    Reprocessed Inquiry Steerable Diagnostics Catheter for electrogram recording and cardiac stimulation during diagnostic electrophysiologic studies; Medline Item Numbers 81102RH 81104RH 81107RH 81174RH 81402RH 81404RH 81405RH 81472RH 81473RH 81474RH 81531RH 81532RH
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2666-2025·2025-10-08

    MAGNETOM Verio Dot Upgrade systems recalled over magnet venting ice blockage

    Siemens is recalling 78 MAGNETOM Verio Dot Upgrade systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.

    Product
    MAGNETOM Verio Dot Upgrade. Model Number: 10684334.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2654-2025·2025-10-08

    Biograph mMR scanners recalled over ice blockage in magnet venting

    Siemens is recalling 27 Biograph mMR systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.

    Product
    Biograph mMR. Model Number: 10433372.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2613-2025·2025-10-08

    Reprocessed cardiac imaging catheters recalled over residual particulates on device surfaces

    Medline is recalling 7,913 reprocessed ViewFlex Xtra ICE catheters because specific lots may carry small residual particulates on patient-contacting surfaces.

    Product
    Reprocessed ViewFlex Xtra ICE Catheter to visualize cardiac structures; blood flow and other devices within the heart. Medline Item Numbers D087031RH
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2661-2025·2025-10-08

    MAGNETOM Skyra fit MRI systems recalled over magnet vent ice blockage

    Siemens is recalling 56 MAGNETOM Skyra fit MRI systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.

    Product
    MAGNETOM Skyra fit. Model Number: 10849580.
    Category
    Medical Device
    Distribution
    Distributed nationwide