The Recall Desk

State

Colorado product recalls

72,940 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 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4326–4350 of 79881

  • HighFDA (Devices)·Z-0584-2026·2025-12-03

    Blood lead test kits recalled over mislabeled calibration buttons

    Magellan Diagnostics is recalling 1,774 LeadCare II Blood Lead Test Kits because calibration buttons used in kitting were labelled with the wrong lot number.

    Product
    The LeadCare¿ II Blood Lead Test System relies on electrochemistry and a unique Sensor to detect lead in whole blood. The LeadCare¿ II Test Kit is provided with the following materials: " Sensors (2 Containers of 24 sensors each; 48 tests) " Treatment Reagent Tubes (2 packag
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0720-2026·2025-12-03

    Anesthesia vaporizers recalled over the potential for anesthesia leakage

    Mindray is recalling 148 Sevoflurane V90 Electronic Vaporizers used with the A9 Anesthesia System over the potential for anesthesia leakage.

    Product
    Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System. Labeled as the following: 1. Sev E_Vap. (Safety Filling adapter), Part Number: 115-066756-00. 2. Exchange Sev E_Vap. (Safety Filling adapter), Part Number: E115-066756-00. Product Description: Th
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0179-2026·2025-12-03

    Saline nasal spray recalled over microbial contamination with Pseudomonas lactis

    Medical Products Laboratories is recalling 41,328 bottles of Walgreens Saline Nasal Spray with Xylitol over microbial contamination identified as Pseudomonas lactis.

    Product
    Walgreens Saline Nasal Spray WITH XYLITOL, 1.5 oz (45mL) bottle, DISTRIBUTED BY: WALGREEN CO., 200 WILMOT RD., DEERFIELD, IL 60015, NDC 0363-3114-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0598-2026·2025-12-03

    Anesthesia set 490469 recalled over backflow and priming occlusion

    B. Braun Medical is recalling 104,784 units anesthesia iv sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.

    Product
    Brand Name: Galaxy System Product Name: Galaxy System Model/Catalog Number: GAL-001 Product Description: The Galaxy SystemTM and its accessories are intended to provide bronchoscopic visualization of and access to patient airways for diagnostic and therapeutic procedure.
    Category
    Medical Device
    Distribution
    20 states
  • HighFDA (Devices)·Z-0589-2026·2025-12-03

    Vena cava filters recalled over resistance when advancing the dilator

    Argon Medical Devices is recalling 1,821 Option ELITE Vena Cava Filter Systems after complaints of increased resistance when advancing the dilator within the introducer sheath.

    Product
    Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated for the prevention of recurrent pulmonary embolism (PE) via percutaneous placement in the inferior vena cava (IVC) in the following conditions: " Pulmonary t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0582-2026·2025-12-03

    Demonstration only gel recalled because it may be placed in patients

    Straumann USA is recalling 61 units of Emdogain because product intended for demonstration purposes only could be placed in patients.

    Product
    Emdogain; Article Numbers: (1) 440.230V10, (2) 475.132V10;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0588-2026·2025-12-03

    Heated massage tables recalled over heat components that can smolder

    Pivotal Health Solutions is recalling 464 Quantum Intersegmental Tables because damage to the heat function components can lead to overheating, smoldering and melting of the vinyl cushion.

    Product
    Quantum Intersegmental Table, Model/Catalog Number: AMQ400H; heated massage table
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V836000·2025-12-03

    Volkswagen ID.4 recalled for high-voltage battery fire risk

    Volkswagen is recalling approximately 629 2023-2024 ID.4 vehicles with defective high-voltage battery cell modules. Misaligned electrodes in the battery may cause fires, posing a risk of injury to vehicle occupants.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID.4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0587-2026·2025-12-03

    Q400 massage tables recalled over heat components that can overheat

    Pivotal Health Solutions is recalling 34 Quantum Intersegmental Tables, model Q400, because damage to the heat function components can lead to overheating and smoldering.

    Product
    Quantum Intersegmental Table, Model/Catalog Number: Q400; heated massage table
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0600-2026·2025-12-03

    Illumination packs recalled because packaging tape contains undisclosed latex

    Stryker is recalling 39,148 NICO Myriad Illumination Packs because tape used to secure components in the packaging contains latex despite the products being labelled latex-free.

    Product
    NICO Myriad Illumination Pack Product No. NN-1000 11g Illumination Sleeve/Fiber; Product No. NN-1001 13g Illumination Sleeve/Fiber
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0599-2026·2025-12-03

    Myriad handpieces recalled because packaging tape contains undisclosed latex

    Stryker is recalling 39,148 NICO Myriad Handpieces because tape used to secure components in the packaging contains latex despite the products being labelled latex-free.

    Product
    NICO Myriad Handpiece Product Number/Product Name: NN-8000 15x10 MHP; NN-8001 15x 13 MHP; NN-8002 15x 25 MHP - MINOP; NN-8003 13x10 MHP; NN-8004 13x13 MHP; NN-8005 15x25 MHP GAAB; NN-8006 11X10 MHP; NN-8007 11x13 MHP; NN-8008 19x28 MHP OI; NN-8010 17x31.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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-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 (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-0191-2026·2025-12-03

    Daily moisturizer recalled over current good manufacturing practice deviations

    CA Botana International is recalling 1,492 tubes of Karina Daily Moisturizer SPF 25 for CGMP deviations.

    Product
    Karina Daily Moisturizer SPF 25, Octinoxate 7.5% and Zinc Oxide 7.0%, Net WT. 5 oz/ 141.7 g per tube, Dist. By: Beauty4Pros LLC, Palm Desert, CA 92211. NDC: 35192-033-16, UPC 8 18204 02572 5
    Category
    Drug
    Distribution
    5 states
  • 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 (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-0194-2026·2025-12-03

    Elixir tinted sunscreen recalled over manufacturing practice deviations

    CA Botana International is recalling Elixir by Coco March Tinted Mineral Sunscreen SPF 50 for CGMP deviations.

    Product
    Elixir by Coco March Tinted Mineral Sunscreen SPF 50, Zinc Oxide 21%, 2.1 oz (62g) per bottle, Distributed by: VitaTienda Co U.S.A., San Juan, PR 00646. NDC: 35192-050-17, UPC 6 7229 99913 8
    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-0185-2026·2025-12-03

    Tea tree balm recalled over current good manufacturing practice deviations

    CA Botana International is recalling 555 tubes of Doctor D. Schwab Controlling Balm with Tea Tree Oil for CGMP deviations.

    Product
    Doctor D. Schwab Controlling Balm with Tea Tree Oil, Salicyclic Acid 0.8%, 1 FL OZ/ 30 ML per tube, Doctor D. Schwab, A division of CA BOTANA, San Diego, CA 92123. NDC: 35192-016-05
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0193-2026·2025-12-03

    Mineral sunscreen recalled over current good manufacturing practice deviations

    CA Botana International is recalling 3,295 bottles of Elixir by Coco March Mineral Sunscreen SPF 50 for CGMP deviations.

    Product
    Elixir by Coco March Mineral Sunscreen SPF 50, Zinc Oxide 21%, 2.1 oz (62g) per bottle, Distributed by: VitaTienda Co U.S.A., San Juan, PR 00646. NDC: 35192-048-17, UPC 8 10145 82007 0
    Category
    Drug
    Distribution
    5 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 (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