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.

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1676–1700 of 89454

  • HighFDA (Food)·H-0803-2026·2026-05-27

    VitaminAlly iron-free women's multivitamin drops recalled over manufacturing deviations

    VitaminAlly Liposomal Women's Liquid Multivitamin Drops, iron free, are being recalled over cGMP deviations that could lead to bacterial pathogen and possible C. botulinum concerns.

    Product
    Liposomal Women's Liquid Multivitamin Drops - Iron Free. Dosage: 3ml Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0790-2026·2026-05-27

    Prostate Bully tonic may be under-processed, allowing botulinum growth

    Prostate Bully in 16 oz and 32 oz bottles is being recalled because it may be under-processed, which could allow growth of Clostridium botulinum, and because it lists health claims.

    Product
    Prostate Bully 16 oz and 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2227-2026·2026-05-27

    Azurion X-ray System Deaeration Hose May Degrade and Cause Oil Leakage

    The deaeration hose in Philips Azurion X-ray tube cooling units may degrade over time and leak oil, affecting cooling performance and automatically triggering low-dose fluoroscopy mode.

    Product
    Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063), Azurion 3 M15 (722064), Azurion 7 B12 (722067), Azurion 7 B20 (722068), Azurion 7 M12 (722078), Azurion 7 M20 (722079, 722224).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2217-2026·2026-05-27

    Medtronic DLP Retrograde Cannula 15FR Model 94665 Sterile Barrier

    Medtronic Perfusion Systems is recalling certain lots of the DLP Retrograde Cannula Model 94665 due to potential sterile barrier breach. The product is used in cardiopulmonary bypass procedures worldwide.

    Product
    Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94665; Cardiopulmonary bypass vascular catheter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2221-2026·2026-05-27

    Medtronic DLP Retrograde Cannula cardiopulmonary bypass catheter

    Medtronic is recalling certain lots of its DLP Retrograde Cannula (Model 94915), a cardiopulmonary bypass vascular catheter, due to potential sterile barrier breach.

    Product
    Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94915; Cardiopulmonary bypass vascular catheter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2214-2026·2026-05-27

    Medtronic GUNDRY Retrograde Cannula Model 94113T sterile barrier recall

    Medtronic is recalling certain lots of GUNDRY Retrograde Cannula (Model 94113T), a cardiopulmonary bypass catheter, due to potential sterile barrier breach in the product.

    Product
    Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T; Cardiopulmonary bypass vascular catheter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0805-2026·2026-05-27

    VitaminAlly liposomal vitamin D3 spray recalled over manufacturing deviations

    VitaminAlly Liposomal D3-5000IU Spray is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.

    Product
    Liposomal D3-5000IU Spray Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2209-2026·2026-05-27

    Tangent Single Use Digital Catheter Recalled for Distal Shaft Fractures

    Tangent Endoscopy is recalling its Tangent Single Use Digital Catheter (models TNG4002-IND and TNG-4007-6pk) due to fractures observed at the distal shaft tip without complete detachment, posing a risk during endoscopic procedures.

    Product
    Tangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers: (1) TNG4002-IND. (2) TNG-4007-6pk.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0806-2026·2026-05-27

    VitaminAlly liposomal D3 and B12 spray recalled over manufacturing deviations

    VitaminAlly Liposomal D3+B12 Spray is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.

    Product
    Liposomal D3+B12 Spray. Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm Address: VitaminAlly LLC Chandler, AZ 85225.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2203-2026·2026-05-27

    Swan-Ganz Jr Catheter models recalled due to lumen hub leakage

    Becton, Dickinson and Company is recalling Swan-Ganz Jr Catheters (models SGPT54, SGPT64P, SGPT755P) because the blue proximal injectate lumen hub may leak or break due to manufacturing changes, risking infection, medication loss, and blood loss.

    Product
    Swan-Ganz Jr Catheter, Models: SGPT54, SGPT64P, SGPT755P
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0794-2026·2026-05-27

    Liquid Blenz Good Brain Tonic may be under-processed, allowing botulinum growth

    Liquid Blenz Good Brain Tonic in 16 oz and 32 oz bottles is being recalled because it may be under-processed, which could allow growth of Clostridium botulinum, and because it lists health claims.

    Product
    Liquid Blenz Good Brain Tonic 16 oz and 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0798-2026·2026-05-27

    VitaminAlly mens liquid multivitamin drops recalled over manufacturing deviations

    VitaminAlly Liposomal Mens Liquid Multivitamin Drops are being recalled over cGMP deviations that could lead to bacterial pathogen and possible C. botulinum concerns.

    Product
    Liposomal Mens Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0782-2026·2026-05-27

    Liquid Blenz Soursop Bitters may be under-processed, allowing botulinum growth

    Liquid Blenz Soursop Bitters in 16 oz and 32 oz bottles is being recalled because it may be under-processed, which could allow growth of Clostridium botulinum, and because it lists health claims.

    Product
    Liquid Blenz Soursop Bitters 16 oz and 32 oz.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0795-2026·2026-05-27

    VitaminAlly Joint Nourish liquid recalled over manufacturing practice deviations

    VitaminAlly Joint Nourish oral liquid is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen contamination and possible C. botulinum concerns.

    Product
    Joint Nourish. Dosage:2 tablespoons (30mL). Liquid. For Oral use. Packaging: Plastic Bottle. Net Volume:480 ml. Firm Address: VitaminAlly LLC Chandler, AZ 85225.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0800-2026·2026-05-27

    VitaminAlly women's multivitamin drops with iron recalled over manufacturing deviations

    VitaminAlly Liposomal Women's Liquid Multivitamin Drops with Iron are being recalled over cGMP deviations that could lead to bacterial pathogen and possible C. botulinum concerns.

    Product
    Liposomal Women's Liquid Multivitamin Drops with Iron. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2229-2026·2026-05-27

    Integris-Allura X-ray systems with degraded deaeration hoses recalled

    Philips is recalling Integris-Allura X-ray systems because deaeration hoses in X-ray tube cooling units may degrade, causing oil leakage that reduces cooling performance and triggers a system shutdown to low-dose mode.

    Product
    Integris-Allura system; System Code Description (Model Numbers): Integris CV Cesar-Powerpack-Visub-Nicol (722030), Integris Allura 15 & 12 (monoplane) (722043), INTEGRIS Allura 15-12 (biplane) (722044), Integris-Allura 9 (722018), Integris-Allura 9 (Biplane) (722021), Integris CV
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0787-2026·2026-05-27

    Immunity Enhancer Elderberry may be under-processed, allowing botulinum growth

    Immunity Enhancer Elderberry in 16 oz and 32 oz bottles is being recalled because it may be under-processed, which could allow growth of Clostridium botulinum, and because it lists health claims.

    Product
    Immunity Enhancer Elderberry 16 oz and 32 oz.
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·26V340000·2026-05-27

    Ford Maverick and Bronco Sport Front Control Arm Ball Joint Detachment Recall

    Ford is recalling certain 2021–2026 Bronco Sport and 2022–2026 Maverick vehicles due to potentially loose or improperly installed front lower control arm ball joints that could disconnect from the wheel knuckle, risking loss of vehicle control and crashes.

    Product
    FORD — FORD MAVERICK, BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2210-2026·2026-05-27

    Oncology Kit With Extension Sets May Leak During Infusion Therapy

    ICU Medical is recalling Oncology Kits with extension sets due to potential leaks that could interrupt chemotherapy infusion and expose hazardous substances to patients, caregivers, and pharmacy technicians.

    Product
    Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros; ChemoLock; Syringe Transfer Set w/MicroClave, ChemoLock Port, REF: CL3960
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2204-2026·2026-05-27

    Swan-Ganz Pacing Catheter Model D200F7 Recall Due to Leak Risk

    Becton, Dickinson and Company is recalling Swan-Ganz Pacing Catheter Model D200F7 due to a manufacturing defect that may cause the proximal injectate lumen hub to leak or break, potentially leading to infection, medication loss, or blood loss.

    Product
    Swan-Ganz Pacing Catheter, Models: D200F7;
    Category
    Medical Device
    Distribution
    Distributed nationwide