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)

Clear filters

2851–2875 of 13446

  • HighFDA (Devices)·Z-2019-2025·2025-07-09

    Siemens ARTIS Angiography Systems Recalled for Rare Dose Reporting Error

    Siemens recalled its ARTIS angiography systems worldwide due to rare communication failures between dose sensors and software that may cause incorrect dose reporting. No illnesses or injuries have been reported.

    Product
    ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed with the ARTIS family include cardiac angiography,
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2069-2025·2025-07-09

    Apex Knee System Recalled for Aged Packaging Material Integrity Loss

    CORIN MEDICAL is recalling 341 units of the Apex Knee System due to aged nylon packaging material that may lose integrity. The systems were distributed nationwide in California, Colorado, Florida, Illinois, Oklahoma, Texas, and Utah.

    Product
    Apex Knee System. Model Numbers: KC-50090, KC-50097, KC-50110, KC-50117, KC-50130, KC-50135, KC-50137, KC-50150, KC-50155, KC-50157, KC-50170, KC-50175, KC-50177, KC-50190, KC-50197, KC-52104, KC-52554, KC-52574, KC-52774, KC-55223, KC-55243
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2054-2025·2025-07-09

    Philips Ultrasound Transducers Recalled: Refurbished Beyond Useful Life

    Philips is recalling 5,230 ultrasound transducers that were refurbished beyond their useful life. Devices may not perform as designed and should not be used.

    Product
    Philips L12-3 Transducer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2062-2025·2025-07-09

    Philips V6-2 Ultrasound Transducers Recalled for Refurbishment Beyond Useful Life

    Philips Ultrasound recalls approximately 5,230 V6-2 ultrasound transducers that were refurbished beyond their useful life. The devices are distributed nationwide and internationally across more than 50 countries.

    Product
    Philips V6-2 Transducer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2067-2025·2025-07-09

    Philips X8-2t Ultrasound Transducers Refurbished Beyond Useful Life

    Philips Ultrasound is recalling approximately 5,230 X8-2t ultrasound transducers that were refurbished beyond their useful life. The devices were distributed nationwide and internationally.

    Product
    Philips X8-2t Transducer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2040-2025·2025-07-09

    VITROS 4600 Chemistry System software defect causes erroneous test results

    Ortho-Clinical Diagnostics is recalling VITROS 4600 Chemistry System analyzers due to a software flaw that can cause test results to be reported using expired reagents. The defect can result in erroneous or delayed test results.

    Product
    Brand Name: VITROS Product Name: VITROS 4600 Chemistry System Model/Catalog Number: (1) 6802445, (2) 6900440 Software Version: version 3.2 to version 3.8.3 (all available software versions) Product Description: In vitro diagnostic chemistry analyzer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2060-2025·2025-07-09

    Philips S7-3t Ultrasound Transducers Refurbished Beyond Useful Life

    Philips is recalling 5,230 S7-3t ultrasound transducers that were refurbished beyond their useful life. Devices operated beyond their intended operational lifespan may not perform reliably.

    Product
    Philips S7-3t Transducer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2048-2025·2025-07-09

    Philips 3D9-3v Ultrasound Transducers Recalled for Refurbishment Beyond Useful Life

    Philips recalls 3D9-3v ultrasound transducers that were refurbished beyond their useful life, risking unreliable device performance. About 5,230 units were distributed nationwide and to 50+ countries.

    Product
    Philips 3D9-3v Transducer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2038-2025·2025-07-09

    VITROS 5600 Integrated System Software Anomaly Causes Erroneous Test Results

    A software anomaly in the VITROS 5600 causes the system to incorrectly treat unexpired reagent packs as expired, potentially producing erroneous test results. The manufacturer is recalling affected units.

    Product
    Brand Name: VITROS Product Name: VITROS 5600 Integrated System Model/Catalog Number: (1) 6802413, (2) 6802915
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2021-2025·2025-07-09

    Interventional fluoroscopic x-ray system may incorrectly report radiation dose

    Siemens interventional x-ray systems may fail to correctly report radiation dose in very rare cases due to sensor-software communication failures. When this occurs, the system incorrectly reports high-dose readings.

    Product
    interventional fluoroscopic x-ray system
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2049-2025·2025-07-09

    Philips C5-1 Ultrasound Transducers Recalled for Refurbishment Beyond Useful Life

    Philips Ultrasound is recalling 5,230 C5-1 ultrasound transducers that were refurbished beyond their useful life, risking device malfunction or degraded diagnostic performance. The devices were distributed nationally and to more than 50 countries.

    Product
    Philips C5-1 Transducer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2075-2025·2025-07-09

    BD Heyman Coude Tip Catheters Recalled for Incorrect French Size Labeling

    C.R. Bard Inc. is recalling BD Heyman Follower Coude Tip catheters (12Fr, 14Fr, 16Fr) due to incorrect French size labeling on product packaging.

    Product
    BD Heyman Follower Coude Tip for following sizes: 12Fr - REF:021312 14Fr - REF:021314, 16Fr - REF: 021316
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2042-2025·2025-07-09

    Surgical Humeral Cup Components Recalled for Missing Quality Inspections

    Onkos Surgical is recalling My3D Personalized Solutions Humeral Cup components used in shoulder replacement surgery because required quality inspections were not performed before release. No injuries have been reported.

    Product
    My3D Personalized Solutions Humeral Cup, Model Number: C24-0223-0003. It is a component of a Custom Constrained Shoulder Arthroplasty Device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2065-2025·2025-07-09

    Philips X6-1 Ultrasound Transducers Recalled for Refurbishment Beyond Useful Life

    Philips Ultrasound is recalling 5,230 X6-1 transducer units that were refurbished beyond their useful life. These devices may not perform reliably due to refurbishment beyond manufacturer specifications.

    Product
    Philips X6-1 Transducer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2022-2025·2025-07-09

    Siemens Interventional Fluoroscopic X-Ray System Dose Reporting Failure

    Siemens interventional fluoroscopic x-ray systems may fail to accurately report applied radiation dose in rare situations due to sensor-software communication failures, potentially providing inaccurate dose information to clinical staff.

    Product
    interventional fluoroscopic x-ray system
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2043-2025·2025-07-09

    IV Catheters in Medline Kits May Fail to Retract During Insertion

    Medline is recalling IV catheters in convenience kits because the needle may be slow to retract or fail to retract during insertion. 186 units were distributed nationwide in six states.

    Product
    Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: 1) CC DRAWER 4 IV CIRCULATION, REF ACC010254B; 2) CC ADULT DRAWER 2, REF ACC010256; 3) PEDI EMERGENCY TRAY-BLUE, REF ACC010316A; 4) ADULT DRAWER 4, REF ACC010389C;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2050-2025·2025-07-09

    Philips Ultrasound C5-2 Transducers Refurbished Beyond Useful Life

    Philips Ultrasound is recalling 5,230 C5-2 Transducers that were refurbished beyond their useful life. The devices may not function reliably and have been distributed nationwide and internationally.

    Product
    Philips C5-2 Transducer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2020-2025·2025-07-09

    Siemens Interventional X-ray System May Misreport Radiation Dose

    Siemens interventional fluoroscopic x-ray systems may fail to correctly measure and report radiation dose due to rare sensor-software communication failures. The worldwide recall affects healthcare facilities using these systems.

    Product
    interventional fluoroscopic x-ray system
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2072-2025·2025-07-09

    Change Healthcare Cardiology Hemodynamics Software May Unexpectedly Shutdown

    Change Healthcare Cardiology Hemodynamics Software version 15.0.1 is being recalled due to complaints that a software update may cause the application to unexpectedly shutdown. The affected software was distributed to 4 systems worldwide.

    Product
    Change Healthcare Cardiology Hemodynamics Software
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2037-2025·2025-07-09

    BiPAP A40 Ventilator Recalled for Improper Respiratory Failure Patient Use

    Philips Respironics BiPAP A40 ventilators are being recalled because they are not indicated for use in patients with respiratory failure. The device may not be appropriate for this patient population.

    Product
    BiPAP A40 Ventilator. Used to provide noninvasive ventilation support for the purpose of treating adult and pediatric patients. BiPAP A40 Pro - sold OUS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2089-2025·2025-07-09

    ADVIA Hematology Analyzer Control Has Incorrect Platelet Values

    Siemens is recalling ADVIA hematology analyzer control products due to incorrect platelet (PLT) value assignments. Approximately 3,266 units are affected, with lot numbers TP253035 and TP253045.

    Product
    ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN2 Control)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2059-2025·2025-07-09

    Philips S7-2 Ultrasound Transducers Recalled: Refurbished Beyond Useful Life

    Philips Ultrasound is recalling 5,230 S7-2 transducers that were refurbished beyond their useful life. The devices were distributed nationwide and internationally and may not function reliably.

    Product
    Philips S7-2 Transducer.
    Category
    Medical Device
    Distribution
    Distributed nationwide