BEUDAMED
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    BD Alaris System; Alaris Syringe Module Model 8110; BD Alaris System; Alaris PCA Module Model 8120; BD Alaris System; Syringe/PCA Sizer Sensor Replacement Kit, P/N 122278652

    FDA Recall
    Open, Classified ·CareFusion 303, Inc.·Product code FRN·August 4, 2020

    PCA 4000 Curing Units, SKU number ACC-06-1000 The PCA 4000 is used for curing industrial resins as well and this recall will not impact units sold to industrial customers.

    FDA Recall
    Open, Classified ·Envisiontec US Llc·Product code EBZ·January 20, 2022

    Alaris PCA Module 8120

    FDA Recall
    Open, Classified ·CareFusion 303, Inc.·Product code FRN·September 15, 2023

    CareFusion Alaris PCA Module, Model 8120

    FDA Recall
    Open, Classified ·CareFusion 303, Inc.·Product code FRN·February 4, 2020

    Alaris PCA Module Model 8120, a modular infusion pump and monitoring system

    FDA Recall
    Open, Classified ·CareFusion 303, Inc.·Product code FRN·August 15, 2024

    LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement Part Number: 6637-0-028

    FDA Recall
    Open, Classified ·Howmedica Osteonics Corp.·Product code JWH·December 1, 2023

    LEFT LARGE-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement Part Number: 6637-0-228

    FDA Recall
    Open, Classified ·Howmedica Osteonics Corp.·Product code JWH·December 1, 2023

    RGT.LARGE-PCA MOD.REV.- DUR.REV.INSERT Intended for knee replacement Product Number: 6637-0-831

    FDA Recall
    Open, Classified ·Howmedica Osteonics Corp.·Product code JWH·December 1, 2023

    RGT.LARGE-PCA MOD.REV.- DUR.REV.INSERT Intended for knee replacement Product Number: 6637-0-928

    FDA Recall
    Open, Classified ·Howmedica Osteonics Corp.·Product code JWH·December 1, 2023

    LEFT LARGE-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement Part Number: 6637-0-231

    FDA Recall
    Open, Classified ·Howmedica Osteonics Corp.·Product code JWH·December 1, 2023

    RGT.LARGE-PCA MOD.REV.- DUR.REV.INSERT Intended for knee replacement. Product Number: 6637-0-931

    FDA Recall
    Open, Classified ·Howmedica Osteonics Corp.·Product code JWH·December 1, 2023

    LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement. Product Number: 6637-0-631

    FDA Recall
    Open, Classified ·Howmedica Osteonics Corp.·Product code JWH·December 1, 2023

    LEFT X-LARGE-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement. Product Number: 6637-0-328

    FDA Recall
    Open, Classified ·Howmedica Osteonics Corp.·Product code JWH·December 1, 2023

    DUR PCA MTK REV INS LFT Intended for knee replacement Product Number: 6728-2-611

    FDA Recall
    Open, Classified ·Howmedica Osteonics Corp.·Product code JWH·December 1, 2023

    DUR PCA MTK REV INS LFT Intended for knee replacement Product Number: 6728-2-609

    FDA Recall
    Open, Classified ·Howmedica Osteonics Corp.·Product code JWH·December 1, 2023

    DUR PCA MTK REV INS RT Intended for knee replacement Product Number: 6728-2-711

    FDA Recall
    Open, Classified ·Howmedica Osteonics Corp.·Product code JWH·December 1, 2023

    DUR PCA MTK REV INS RT Intended for knee replacement Product Number: 6728-2-709

    FDA Recall
    Open, Classified ·Howmedica Osteonics Corp.·Product code JWH·December 1, 2023

    Arrow Pressure Injectable Arrowg+ard Blue Plus Four-Lumen CVC, REF CDC-45854-P1A; catheter, intravascular, therapeutic, long-term greater than 30 days

    FDA Recall
    Open, Classified ·ARROW INTERNATIONAL Inc.·Product code FOZ·August 10, 2023

    Impella CP Pump Set, Japan; Product Code: 0048-0034-JP;

    FDA Recall
    Open, Classified ·Abiomed, Inc.·Product code OZD·August 5, 2024

    Impella CP Smart Assist Set, JP; Product Code: 0048-0024-JP;

    FDA Recall
    Open, Classified ·Abiomed, Inc.·Product code OZD·August 5, 2024