24 results · 14ms · Sources: EU EUDAMED, US FDA

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Catalog Number: 900010 SUTURE REMOVAL KIT Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc.

FDA Recall
Terminated ·Customed, Inc Calle Igualdad Final # 7·Product code MCZ·January 7, 2016

Achillon minimally invasive Achilles tendon suture system

FDA Recall
Terminated ·Wright Medical Technology Inc·Product code MCZ·July 2, 2004

Skin Stapler Removal Kit , catalog# 900-782

FDA Recall
Terminated ·Customed, Inc Calle Igualdad Final # 7·Product code MCZ·December 8, 2011

Surgical packs (includes trays, bags and kits) Used by medical staff to perform patient care procedures such as wound healing, suture removals, irrigate wounds, etc.

FDA Recall
Terminated ·Customed, Inc Calle Igualdad Final # 7·Product code MCZ·October 8, 2014

SKIN STAPLE REMOVER

FDA Recall
Terminated ·Centurion Medical Products Corporation·Product code MCZ·October 23, 2017

SUTURE REMOVAL KIT CUSTOMED 100/CS Used by medical staff to perform patient care procedures such as wound healing, suture removals, irrigate wounds, etc.

FDA Recall
Terminated ·Customed, Inc Calle Igualdad Final # 7·Product code MCZ·July 10, 2015

Tri-State Centurion Plastic Laceration Set, sterile, 16 per case, Tri-State Hospital Supply Corp., Howell, MI; Reorder SUT3390.

FDA Recall
Terminated ·Tri-State Hospital Supply Corporation·Product code MCZ·January 14, 2009

Laceration/Suture Removal, Sterile Single Use, Latex Free, 20/case, Medical Action Industries, Inc, Arden, NC.

FDA Recall
Terminated ·Medical Action Industries Inc·Product code MCZ·June 12, 2014

Suture removal kit, catalog# 900-010

FDA Recall
Terminated ·Customed, Inc Calle Igualdad Final # 7·Product code MCZ·December 8, 2011

Tri-State Centurion Laceration Tray - SnagFree, sterile, 16 per case, Tri-State Hospital Supply Corp., Howell, MI; Reorder SUT12265.

FDA Recall
Terminated ·Tri-State Hospital Supply Corporation·Product code MCZ·January 14, 2009

SUTURE REMOVAL TRAY, SET or KIT

FDA Recall
Terminated ·Centurion Medical Products Corporation·Product code MCZ·October 23, 2017

Flexicair MC3 (model M4000) Low Airloss Therapy Units, for the prevention of pressure sores.

FDA Recall
Terminated ·Hill-Rom Manufacturing, Inc.·Product code IOQ·May 12, 2009

FLEXICAIR MC3 Low Airloss Therapy unit

FDA Recall
Terminated ·Hill-Rom Manufacturing, Inc.·Product code IOQ·August 27, 2003

Power electronic box, Part #AS-0066, subassembly for the MyoCycle MC-2.

FDA Recall
Terminated ·Myolyn Inc.·Product code GZI·July 19, 2022

Flexicair II (model 13000) Low Airloss Therapy Units, for the prevention of pressure sores.

FDA Recall
Terminated ·Hill-Rom Manufacturing, Inc.·Product code IOQ·May 12, 2009

Flexicair MC3 (Model number: M4000) Low Airloss Therapy Units For use to prevent pressure sore development and wound deterioration in patients who have significant risk of developing these problems and who generally also have one or more to the following conditions: immobility, incontinence, poor nutrition, diminished level of consciousness, reduced subcutaneous tissue, or multi-system failure.

FDA Recall
Terminated ·Hill-Rom Manufacturing, Inc.·Product code IOQ·December 6, 2010

FLEXICAIR II, Low Airloss Therapy unit.This unit is similar to MC3 but does not have the utility shelf above the foodboard, patient scale or alternate CPR function actuators.

FDA Recall
Terminated ·Hill-Rom Manufacturing, Inc.·Product code IOQ·August 27, 2003

NUVASIVE MAGEC 2 Rod X.X mm XX mm, REF MC2-XXXXS LOT 0000000 AAA - Product Usage: comprised of a sterile single-use spinal rod that is surgically implanted using appropriate NuVasive Reline, Reline Small Stature, and Armada fixation components (i.e. Pedicle screws, hooks and/or connectors, provided non-sterile, to be sterilized by the end user).

FDA Recall
Terminated ·NuVasive Inc·Product code PGN·February 13, 2020

Flexicair II (Model number 13000) Low Airloss Therapy Units For use to prevent pressure sore development and wound deterioration in patients who have significant risk of developing these problems and who generally also have one or more to the following conditions: immobility, incontinence, poor nutrition, diminished level of consciousness, reduced subcutaneous tissue, or multi-system failure.

FDA Recall
Terminated ·Hill-Rom Manufacturing, Inc.·Product code IOQ·December 6, 2010

Centurion-Trays EBSI1021 VALVE CHANGE KIT- DOUBLE

FDA Recall
Terminated ·Centurion Medical Products Corporation·Product code KCZ·December 11, 2019