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 the agency’s own highest classification or reported deaths or serious injuries, 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.

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6551–6575 of 114917

  • HighFDA (Devices)·Z-0583-2026·2025-12-03

    Skin cancer aid recalled because it may not meet specifications

    DermaSensor is recalling nine affected units of its software-aided diagnostic device because it may not meet specifications, risking incorrect results or a delayed referral.

    Product
    DermaSensor. Model/Catalog Number: 10101. Software Version: 3.0.2. Software-aided adjunctive diagnostic device for use by physicians on lesions suspicious for skin cancer
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0609-2026·2025-12-03

    Anesthesia set 490477 recalled over backflow and inability to prime

    B. Braun Medical is recalling 36,552 units anesthesia iv 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…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0683-2026·2025-12-03

    IV set 354211 recalled over piggyback backflow and occlusion risk

    B. Braun Medical is recalling 286,400 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 ADM 15 DROP W/3…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0696-2026·2025-12-03

    IV set 490437 recalled over piggyback backflow and occlusion risk

    B. Braun Medical is recalling 4,536 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 ADMIN SET W/ 15…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0617-2026·2025-12-03

    Blood set 490355 recalled over backflow into the primary container

    B. Braun Medical is recalling 24,624 units blood administration sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.

    Product
    Blood 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. Y-TYPE BLOOD SET W/ 170…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0660-2026·2025-12-03

    IV set 490343 recalled over piggyback backflow and priming occlusion

    B. Braun Medical is recalling 1,272 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 ADMIN SET,2 CARESITE…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0655-2026·2025-12-03

    IV set 457504 recalled over medication backflow and priming failure

    B. Braun Medical is recalling 80,650 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 SET W/2 CARESITE & 2…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0707-2026·2025-12-03

    Outlook set 354213 recalled over backflow into the primary container

    B. Braun Medical is recalling 18,072 units outlook 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 IV SET 15DROP W/3 CARESITE…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0625-2026·2025-12-03

    Caresite set 354202 recalled over backflow and inability to prime

    B. Braun Medical is recalling 2,871,707 units caresite sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.

    Product
    Caresite 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 numbers: 1. Primary Gravity IV Set with 2…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0602-2026·2025-12-03

    Respiratory test panels recalled over elevated risk of false negative results

    BioFire Diagnostics is recalling 23 kits of the BioFire Respiratory Panel 2.1 because unintended movement of pouch chemistry may cause false negative results and control failures.

    Product
    BioFire Respiratory Panel 2.1, IVD, REF: 423742 (30 test kit)
    Category
    Medical Device
    Distribution
    11 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…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0723-2026·2025-12-03

    Imaging software recalled over a bug that can lose clinical information

    Intelerad Medical Systems is recalling 19 IntelePACS InteleConnect and TechPortal installations because a bug can cause data loss in the Relevant Clinical Info field.

    Product
    IntelePACS - InteleConnect / TechPortal
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0606-2026·2025-12-03

    Anesthesia set 490189 recalled over piggyback backflow and occlusion risk

    B. Braun Medical is recalling 32,436 anesthesia IV 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…
    Category
    Medical Device
    Distribution
    0 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-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 (Drugs)·D-0192-2026·2025-12-03

    Tinted mineral sunscreen recalled over manufacturing practice deviations

    CA Botana International is recalling 2,090 tubes of Sugared+Bronzed Tinted Mineral Sunscreen SPF 50 for CGMP deviations.

    Product
    Sugared+Bronzed Tinted Mineral Sunscreen SPF 50, Zinc Oxide 21%, Net WT 3.3 OZ (93 G) per tube, Dist. By: Sugared+Bronzed, 929 Montana Ave, Santa Monica, CA 90403. NDC: 35192-055-18, UPC 8 50047 92223 6
    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-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-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 (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 (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…
    Category
    Medical Device
    Distribution
    0 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