The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Filters

Agency

All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

5476–5500 of 113838

  • HighFDA (Devices)·Z-0638-2026·2025-12-03

    Caresite extension sets recalled over piggyback backflow and occlusion

    B. Braun Medical is recalling 32,500 Caresite extension sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.

    Product
    Extension Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. Caresite Extension Set_Export; Cata
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0639-2026·2025-12-03

    Extension set V5405 recalled over backflow and inability to prime

    B. Braun Medical is recalling 300 units extension sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.

    Product
    Extension Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. EXT/2INJ/FLBL/FML LRLK/CV 34; Catal
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0607-2026·2025-12-03

    IV set 477002 recalled over backflow from secondary piggyback containers

    B. Braun Medical is recalling 22,928 units iv administration sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.

    Product
    Anesthesia IV Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET W/15 DROPS/ML, 132
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0662-2026·2025-12-03

    IV set 490367 recalled over medication backflow and priming failure

    B. Braun Medical is recalling 6,768 IV administration sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.

    Product
    IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET W/60 DR/ML, CA
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0708-2026·2025-12-03

    Outlook pump sets recalled over backflow into the primary container

    B. Braun Medical is recalling 2,352 Outlook pump sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.

    Product
    Outlook set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. OUTLOOK PUMP SET 3 CARESITE LADS 133
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0652-2026·2025-12-03

    IV set 490241 recalled over backflow and inability to prime

    B. Braun Medical is recalling 66,792 IV administration sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.

    Product
    IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET HF STOPCOCK,10
    Category
    Medical Device
    Distribution
    0 states
  • 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-0615-2026·2025-12-03

    IV set 490349 recalled over backflow from secondary piggyback containers

    B. Braun Medical is recalling 24,648 IV administration sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.

    Product
    B.BRAUN utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET W/ 60 DROPS/ML,141 in.; Cata
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0654-2026·2025-12-03

    IV set 354210 recalled over backflow and inability to prime

    B. Braun Medical is recalling 1,861,111 units iv administration sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.

    Product
    IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ANES 15DROP W/2 CARESITE
    Category
    Medical Device
    Distribution
    0 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+ B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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-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 (Devices)·Z-0666-2026·2025-12-03

    Liquid biopsy reports recalled for omitting the companion diagnostic claims page

    Foundation Medicine is recalling 18 FoundationOne Liquid CDx reports that were sent to customers without the companion diagnostic Claims Page.

    Product
    IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET W/15 DROPS/ML,
    Category
    Medical Device
    Distribution
    0 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
  • ModerateFDA (Drugs)·D-0187-2026·2025-12-03

    Mineral sunscreen recalled over current good manufacturing practice deviations

    CA Botana International is recalling 874 tubes of Sea Enzyme Ultra Umbrella Sunscreen SPF 30 for CGMP deviations.

    Product
    Sea Enzyme Ultra Umbrella Sunscreen SPF 30, Titanium Dioxide 4%, Octinoxate 4%, 4 oz./113.4 g per tube, Manufactured by CA BOTANA, San Diego, CA 92121. NDC: 35192-011-02
    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 (Devices)·Z-0656-2026·2025-12-03

    Bronchoscopy robots recalled because the user manual was password protected

    Noah Medical is recalling 47 Galaxy Systems because users did not have access to the Instructions for Use and User Manual, which was password protected.

    Product
    IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET W/15 DROPS/ML
    Category
    Medical Device
    Distribution
    0 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-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-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-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-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-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