BEUDAMED
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    SIGMA HP MBT Non-Keel Punch Knee Instrument. Designed to be used as an option in stabilizing the tibial trial during trial reduction.

    FDA Recall
    Terminated ·DePuy Orthopaedics, Inc.·Product code LRY·January 8, 2016

    JUGGERKNOT INGUIDE PUNCH, 2.9MM. The JuggerKnot 2.9mm In-Guide Punch is intended to be used to prepare a 2.9mm hole into bone in which the JuggerKnot 2.9mm Suture Anchor is to be placed. The JuggerKnot 2.9mm Suture Anchor is intended to be used to attach soft tissue to bone.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code LRY·August 14, 2012

    HealthLink***BIOPSY PUNCHES*** Disposable manual instrument for skin biopsy.

    FDA Recall
    Terminated ·Clorox Healthcare Holdings, LLC (dba HealthLink) 3611 Saint Johns Bluff Rd S Ste 1 Suite 1 Jacksonville FL 32224-2679·Product code LRY·March 18, 2013

    PSS Select medical products***Biopsy Punches*** Disposable manual instrument for skin biopsy.

    FDA Recall
    Terminated ·Clorox Healthcare Holdings, LLC (dba HealthLink) 3611 Saint Johns Bluff Rd S Ste 1 Suite 1 Jacksonville FL 32224-2679·Product code LRY·March 18, 2013

    ARGENT SURGICAL SYSTEMS***BIOPSY Punches*** Disposable manual instrument for skin biopsy.

    FDA Recall
    Terminated ·Clorox Healthcare Holdings, LLC (dba HealthLink) 3611 Saint Johns Bluff Rd S Ste 1 Suite 1 Jacksonville FL 32224-2679·Product code LRY·March 18, 2013

    Surgical punch; sealed pouches packed in punch shelf box Intended for use by trained surgeons to create circular cuts in soft tissue or openings in soft vessel walls during surgical procedures.

    FDA Recall
    Terminated ·Alto Development Corp·Product code LRY·October 23, 2017

    ARIES System and ARIES M1 System

    FDA Recall
    Terminated ·Luminex Corporation·Product code OOI·April 19, 2017

    Luminex Aries M1 System Model: Aries M6V1 Aries Software v1.0 For In Vitro Diagnostic Use in clinical laboratories. Scanner Label/Labeling: JADAK JDK-2330 REV B 170512-017

    FDA Recall
    Terminated ·Luminex Corporation·Product code OOI·June 29, 2018

    ARIES HSV 1&2 Assay, Part Number/REF 50-10017

    FDA Recall
    Terminated ·Luminex Corporation·Product code OOI·April 16, 2021

    HSG Trays/HS 5F Catheter Combo; HSG Procedure Tray+ Shapeable 5F HSG catheter. For hysterosonography and hysterosalpingography, gynecological use.

    FDA Recall
    Terminated ·Catheter Research, Inc·Product code HGS·April 7, 2015

    ARIES Extraction Kit; ARIES System; SYNCT , REF 50-10026, UDI # 00840487100073

    FDA Recall
    Open, Classified ·Luminex Corporation·Product code OOI·February 20, 2019

    ARIES HSV 1&2 Assay, Catalog/REF# 50-10017

    FDA Recall
    Terminated ·Luminex Corporation·Product code OOI·November 17, 2021

    Siemens syngo.plaza VA20A Server Farm setup integrated to a RIS, model number 10592457.

    FDA Recall
    Terminated ·Siemens Medical Solutions USA, Inc·Product code LLZ·May 1, 2011

    Syngo Imaging Version Lines VB20, VB30, VB35 in combination with a RIS.

    FDA Recall
    Terminated ·Siemens Medical Solutions USA, Inc·Product code LLZ·April 6, 2010

    ARIES SARS-CoV-2 Assay

    FDA Recall
    Open, Classified ·Luminex Corporation·Product code QJR·July 14, 2022

    Aries Bordetella Assay, REF 50-10037, UDI # 00840487101452

    FDA Recall
    Open, Classified ·Luminex Corporation·Product code OZZ·February 20, 2019

    ARIES SARS-CoV-2 Assay, REF: 50-10047

    FDA Recall
    Open, Classified ·Luminex Corporation·Product code QJR·September 14, 2022

    ARIES GBS Assay , REF 50-10021, UDI # 00840487100165

    FDA Recall
    Open, Classified ·Luminex Corporation·Product code NJR·February 20, 2019

    ARIES HSV 1&2 Assay , REF 50-10017, UDI # 00840487100295

    FDA Recall
    Open, Classified ·Luminex Corporation·Product code PGI·February 20, 2019

    ARIES C. difficile Assay , REF 50-10018, UDI # 00840487100059

    FDA Recall
    Open, Classified ·Luminex Corporation·Product code OZN·February 20, 2019