BEUDAMED
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    MassChrom Cortisol, Cortisone Saliva Control Level II, Order No. 0350 - Product Usage: The kit is used as a test for patients to monitor their cortisol and cortisone levels.

    FDA Recall
    Completed ·Chromsystems Instruments & Chemicals GmbH Am Haag 12 Grafelfing Germany·Product code JJY·October 29, 2020

    MassChrom Cortisol, Cortisone Saliva Control Level I, Order No. 0349 - Product Usage: The kit is used as a test for patients to monitor their cortisol and cortisone levels.

    FDA Recall
    Completed ·Chromsystems Instruments & Chemicals GmbH Am Haag 12 Grafelfing Germany·Product code JJY·October 29, 2020

    6PLUS1 Multilevel Saliva Calibrator Set Cortisol Cortisone in Saliva, Order No. 73039 - Product Usage: The kit is used as a test for patients to monitor their cortisol and cortisone levels.

    FDA Recall
    Completed ·Chromsystems Instruments & Chemicals GmbH Am Haag 12 Grafelfing Germany·Product code JIX·October 29, 2020

    LEGION(TM) HEMI STEP TIBIAL WEDGE RK/HK, 5 MM, SIZE 3-4 LT.MDL/RT-LAT, REF 71423432 Product Usage: The constrained knee systems are designed for use in patients in primary and revision surgery, where the posterior cruciate ligament and one or both of the collateral ligaments (i.e., medial collateral and/or lateral collateral ligament) are absent or incompetent.

    FDA Recall
    Completed ·Smith & Nephew, Inc.·Product code JWH·January 15, 2018

    Protege GPS Self-Expanding Peripheral Stent System, product number SERB65-09-60-80, Sterile.

    FDA Recall
    Completed ·Medtronic Inc.·Product code NIP·November 20, 2023

    illumina Model NextSeq 550 Dx REF 20005715

    FDA Recall
    Completed ·Illumina, Inc.·Product code PFF·May 3, 2022

    illumina REF DX-410-1001 Model: MiSeq Dx illumina REF 15036706 Model: MiSeq Dx illumina REF 20014053 Model: MiSeq Dx

    FDA Recall
    Completed ·Illumina, Inc.·Product code PFF·May 3, 2022

    LINQ II Insertable Cardiac Monitor

    FDA Recall
    Completed ·Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)·Product code MXD·January 18, 2022

    PTS Panels CHOL+GLU Test Strips (REF 1765)

    FDA Recall
    Completed ·Polymer Technology Systems, Inc. dba PTS Diagnostics, Inc.·Product code CGA·August 16, 2022

    TrueDent Cyan, TDM 120, Model No. OBJ-09165 Light-curable methacrylate-based resin that enables fabrication of dental appliances

    FDA Recall
    Completed ·STRATASYS LTD·Product code EBI·January 19, 2024

    TrueDent Magenta, TDM130, Model No. OBJ-09166 Light-curable methacrylate-based resin that enables fabrication of dental appliances

    FDA Recall
    Completed ·STRATASYS LTD·Product code EBI·January 19, 2024

    TrueDent White, TDM110, Model No. OBJ-09168 Light-curable methacrylate-based resin that enables fabrication of dental appliances

    FDA Recall
    Completed ·STRATASYS LTD·Product code EBI·January 19, 2024

    TrueDent Clear, TDM 100, Model No. OBJ-09164 Light-curable methacrylate-based resin that enables fabrication of dental appliances

    FDA Recall
    Completed ·STRATASYS LTD·Product code EBI·January 19, 2024

    TrueDent Yellow, TDM140, Model No. OBJ-09169 Light-curable methacrylate-based resin that enables fabrication of dental appliances

    FDA Recall
    Completed ·STRATASYS LTD·Product code EBI·January 19, 2024

    Destino Twist 14F (also branded as Guidestar 14F)

    FDA Recall
    Completed ·Oscor Inc.·Product code DYB·December 22, 2021

    NEO-KATH Epidural Catheter Set, REF 200-2430, Sterile

    FDA Recall
    Completed ·Epimed International·Product code BSO·December 28, 2017

    Immundiagnostik IDK Lactoferrin ELISA- In vitro enzyme immunoassay intended for the determination of lactoferrin in stool. P/N: K6870 Single Kit P/N: K6870.20.US.L 20 Plates

    FDA Recall
    Completed ·IMMUNDIAGNOSTIK, Inc·Product code DEG·March 27, 2023

    NEO-KATH(TM) Caudal Set, REF 201-2430, Sterile

    FDA Recall
    Completed ·Epimed International·Product code BSO·December 28, 2017

    1.8mm Truss Wire, REF: 900217, a Component of Metalogix Revolution External Plating System

    FDA Recall
    Completed ·New Standard Device Inc·Product code KTT·June 8, 2020

    Delta Cup Beater Positioner - Aligner, model # 9057.20.555 Used during implantation of the Delta Acetabular System

    FDA Recall
    Completed ·Limacorporate S.p.A Via Nazionale 52 Frazione Villanova San Daniele del Friuli Italy·Product code LXH·September 8, 2017