The Recall Desk

State

Colorado product recalls

73,738 recalls have nationwide distribution and so reach Colorado. 6,951 additional recalls listed Colorado specifically in their distribution scope.

What the numbers show

Total
6,951
Critical
1,215
Severe
1,826
Most recent
2026-10-28

Of the 6,951 recalls naming Colorado we have scored against our rubric, 1,215 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,826 (26%) are Severe.

These figures cover only the 6,951 recalls whose distribution notice names Colorado specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5151–5175 of 80689

  • ModerateFDA (Devices)·Z-0585-2026·2025-12-03

    Culture media recalled over contamination that may darken the broth

    Remel is recalling cation-adjusted Mueller Hinton broth and Brucella broth because the products may contain contamination, which may result in a darker or brown media color.

    Product
    1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0190-2026·2025-12-03

    Gabriel mineral sunscreen recalled over manufacturing practice deviations

    CA Botana International is recalling 1,617 tubes of Gabriel Mineral Sunscreen SPF 50 for CGMP deviations.

    Product
    Gabriel Mineral Sunscreen SPF 50, Zinc Oxide 21%, 2.1 oz, Net 61 g per tube, Dist. By: Gabriel Cosmetics, Inc., Redmond, WA USA 98052, NDC: 35192-044-01, UPC 7 07060 9592 1
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-0719-2026·2025-12-03

    Interventional imaging systems recalled over ceiling rail movement that may fail

    Philips is recalling 172 Azurion 7M20 systems with FlexArm because motorized longitudinal movement of the stand may be inconsistent and eventually become unavailable.

    Product
    Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model Number: 722234;
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Drugs)·D-0196-2026·2025-12-03

    Menthol pain relief gel recalled over manufacturing practice deviations

    CA Botana International is recalling 4,890 bottles of Dr. Bump Natural Pain Relief Gel with Menthol 5% for CGMP deviations.

    Product
    Dr. Bump Natural Pain Relief Gel, Menthol 5%, NET WT 4 FL OZ/118 ML per bottle, Distr. by 1Beauty US LLC, Palm Desert, CA 92211. NDC: 35192-052-18, UPC 8 18204 02513 8
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0195-2026·2025-12-03

    CLEARSTEM sunscreen recalled over current good manufacturing practice deviations

    CA Botana International is recalling 4,890 bottles of CLEARSTEM You Are Sunshine SPF 50 for CGMP deviations.

    Product
    CLEARSTEM YOU ARE SUNSHINE SPF 50, Zinc Oxide 21%, 2.1 oz/61g per bottle, Distributed by: CLEARSTEM Skincare, clearstemskincare.com. NDC: 35192-046-17
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0189-2026·2025-12-03

    Shimmery sun lotion recalled over current good manufacturing practice deviations

    CA Botana International is recalling 805 tubes of Doctor D. Schwab Shimmery Sun Lotion Sunscreen SPF 30 for CGMP deviations.

    Product
    Doctor D. Schwab Shimmery Sun Lotion Sunscreen SPF 30, Titanium Dioxide 5% and Octinoxate 4%, 4 oz./113.4 g per tube, Doctor D. Schwab, A division of CA BOTANA, San Diego, CA 92121. NDC: 35192-012-02
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0184-2026·2025-12-03

    Tinted moisturizer SPF 50 recalled over manufacturing practice deviations

    CA Botana International is recalling 1,401 tubes of Doctor D. Schwab Flawless Skin Fluid Tinted Moisturizer SPF 50 for CGMP deviations.

    Product
    Doctor D. Schwab Flawless Skin Fluid Tinted Moisturizer SPF 50, Zinc Oxide 21%, 2.1 oz/61 g per tube, Manufactured by CA BOTANA, San Diego, CA 92121. NDC: 35192-043-17
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0188-2026·2025-12-03

    Menthol arnica gel recalled over current good manufacturing practice deviations

    CA Botana International is recalling 810 tubes of Doctor D. Schwab Clinical Weh Weh Natural Pain Relief Gel with Menthol and Arnica for CGMP deviations.

    Product
    Doctor D. Schwab Clinical Weh Weh Natural Pain Relief Gel with Menthol and Arnica, Menthol 5%, 4.2 oz./120 g per tube, Doctor D. Schwab, A division of CA BOTANA, San Diego, CA 92121. NDC: 35192-020-02
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0183-2026·2025-12-03

    Schwab mineral sunscreen recalled over manufacturing practice deviations at Botana

    CA Botana International is recalling 1,167 tubes of Doctor D. Schwab Mineral Sunscreen SPF 50 for CGMP deviations.

    Product
    Doctor. D. Schwab Mineral Sunscreen SPF 50, Zinc Oxide 21%, 4 oz./ 113.4 g per tube, Manufactured by CA Botana, San Diego, CA 92123. NDC: 35192-042-02
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0186-2026·2025-12-03

    Benzoyl peroxide cream recalled over current good manufacturing practice deviations

    CA Botana International is recalling 470 tubes of Doctor D. Schwab Controlling Cream with Benzoyl Peroxide 2.7% for CGMP deviations.

    Product
    Doctor D. Schwab Controlling Cream, Benzoyl Peroxide 2.7%, 1 FL OZ/ 30 ML per tube, Doctor D. Schwab, A division of CA BOTANA, San Diego, CA 92123. NDC: 35192-017-05
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-0581-2026·2025-12-03

    Vitrectomy probe packs recalled with no reason stated in the record

    Alcon Research is recalling 28,323 Constellation UltraVit 10K and HyperVit 20K vitrectomy probe packs; the enforcement record does not state a reason.

    Product
    CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K, Description/REF: 25+ TOTALPLUS CP PAK 20K CPM BWV .9 IU/ 8065000093; 25+ TOTALPLUS CP PAK 20K CPM BV .9 IU/ 8065000095; 27+ TOTALPLUS CP PAK 20K CPM BV .9 IU/ 8065000096; 23GA BEVEL ULTRAVIT 10,000 CPM/ 8065752413; 25+…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V834000·2025-12-02

    Zero Recalls 2023 DSR/X Motorcycles Due to Motor Controller Defect

    Zero Motorcycles is recalling 2023 DSR/X motorcycles because incorrect fasteners in the motor controller may cause a loss of drive power, increasing crash risk.

    Product
    ZERO — ZERO DSR/X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V824000·2025-12-01

    2019 Ram Trucks Recalled for Side Curtain Air Bag Inflator Defect

    Chrysler is recalling 2019 Ram 1500, 2500, and 3500 vehicles because side curtain air bag inflators may rupture, potentially sending metal fragments into the cabin.

    Product
    RAM — RAM 3500, 2500, 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V828000·2025-12-01

    Ford Recalls 2025 Maverick for Cylinder Head Manufacturing Defect

    Ford is recalling 2025 Maverick vehicles with defectively manufactured cylinder heads that can leak oil. The leak increases the risk of fire and engine failure.

    Product
    FORD — FORD, LINCOLN EXPLORER, MUSTANG, MAVERICK, CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V832000·2025-12-01

    Virnig Recalls 2025 Trailers Due to Bearing Lock Nut Failure Risk

    Virnig is recalling 2025 TR-HDD-1414 and TR-RHDD-1409 trailers because improperly installed bearing lock nuts may fail, causing the tire to detach and increasing crash risk.

    Product
    VIRNIG — VIRNIG TR-HDD-1414, TR-RHDD-1409
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V827000·2025-12-01

    Ford Recalls 2016-2019 Lincoln MKT for Detaching B-Pillar Trim

    Ford is recalling 2016-2019 Lincoln MKT vehicles because the B-pillar door trim may detach while driving, creating a road hazard and increasing crash risk.

    Product
    LINCOLN — LINCOLN MKT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V823000·2025-12-01

    2025 Ford Expedition and Other Models Recalled for Brake Booster Malfunction

    Ford is recalling 679 2025 Expedition, Ranger, F-150, Bronco, and Navigator vehicles due to a potential Electronic Brake Booster malfunction that can cause loss of power brake assist, increasing crash risk.

    Product
    FORD — FORD, LINCOLN F-150, EXPEDITION, BRONCO, RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V825000·2025-12-01

    KTM and Husqvarna motorcycles recalled for engine control software stalling defect

    KTM and Husqvarna are recalling certain 2024-2025 motorcycles because faulty engine control software may cause the engine to stall at low RPMs, creating a risk of crashes.

    Product
    KTM — KTM, HUSQVARNA 390 DUKE, 390 ADVENTURE R, SVARTPILEN 401, VITPILEN 401
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V831000·2025-12-01

    2025 Lincoln Navigator Rear Lightbar Cracks May Disable Reverse Lights

    Ford is recalling certain 2025 Lincoln Navigator vehicles. The rear lightbar may develop cracks allowing moisture accumulation, potentially disabling reverse lights and reducing visibility when backing up.

    Product
    LINCOLN — LINCOLN NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V829000·2025-12-01

    2025 Ford Escape liftgate hinge covers may detach, creating crash risk

    Ford is recalling certain 2025 Escape vehicles because liftgate hinge covers may not be properly secured and can detach. Detached covers can create a distraction or road hazard, increasing crash risk.

    Product
    FORD — FORD ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V826000·2025-12-01

    2025-2026 RAM Pickup Trucks: Blank Instrument Panel Display Software Error

    Chrysler is recalling 2025-2026 RAM pickup trucks (1500, 2500, 3500, 4500, 5500) because a software error causes the instrument panel display to go blank, preventing drivers from seeing critical warning lights and gear selection.

    Product
    RAM — RAM 1500, 2500, 3500, 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V833000·2025-12-01

    Genesis G90 Models: Highway Drive Assist Braking Malfunction Recall

    Hyundai is recalling 2023-2026 Genesis G90 vehicles because the Highway Drive Assist radar may falsely detect another vehicle, causing sudden braking that increases crash risk.

    Product
    GENESIS — GENESIS G90
    Category
    Vehicle
    Distribution
    Distributed nationwide