BEUDAMED
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    SURGICAL MEDICAL DEVICE CAUTERY

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    SMARTLOCK

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·37613154184508·Locking Screws, Cross-Pin

    YELLOW SPECIAL

    FDA 510(k)
    FDA Class 2 ·Dental

    MICROSCAN SYNERGIES PLUS GRAM-NEGATIVE MIC/COMBO PANELS WITH CEFTRIAXONE (0.5-128 UG/ML)

    FDA 510(k)
    FDA Class 2 ·Microbiology

    PERFORMANCE TOTAL KNEE PROSTHESIS

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code HRY·October 25, 2019

    PERFORMANCE DISTAL FAB LM/RL MED

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code JWH·October 18, 2016

    PERFORMANCE DISTAL FAB LL/RM MED

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code JWH·October 18, 2016

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·January 28, 2025

    VANGRD CR POR/HA FEM - RT 72.5

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·March 31, 2016

    TINBN VNGRD INT CR ANAT FEMORAL R 62.5 MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·March 31, 2016

    VANGUARD CR POROUS/HA FEM - RT 72.5

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·March 23, 2016

    PINNACLE MTL INS NEUT36IDX54OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·March 27, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 1, 2011

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·PURITAN-BENNETT CORP·Product code CBK·April 2, 2008

    VANGUARD CEMENTLESS POROUS CR FEMORAL LT 65

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·April 20, 2017

    VANGUARD CRUCIATE RETAINING POROUS HA FEMUR - RIGHT 65 MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·May 12, 2017

    Advisor Vital Signs Monitor (model 9200), catalog number 925754220, with Impedance Respiration board (optional circuit board, P/N: 80004B1) installed manufactured with Rev 10 Main boards (P/N: 80002B1) CE/MDD marking, 5-lead 60 Hz ECG and standard SPO2 option.

    FDA Recall
    Terminated ·Smiths Medical PM, Inc.·Product code DPS·September 1, 2005

    Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

    FDA Enforcement
    Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012

    The Spirit Select Bed, Model 5700 Spirit Plus /with high rail siderail option

    FDA Enforcement
    Class II ·Terminated·Stryker Medical Division of Stryker Corporation·November 21, 2018