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LCP DRILL SLEEVE 3.5 F/DRILL BITS Ø2.8

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code FZX·June 4, 2013

3:1 Dermacarrier, Model Number 00219501300, skin graft carrier

FDA Recall
Open, Classified ·Zimmer Surgical Inc·Product code FZW·January 2, 2024

CONCEPT GRAFIX TENDON STRIPPER. REF TS8850. 7.0MM, QTY 1. Rx Only, Non-Sterile, Made In USA.

FDA Recall
Terminated ·Linvatec Corp. dba ConMed Linvatec·Product code FZW·January 29, 2010

Zimmer Dermacarriers II skin graft carriers, 9 to 1 dermacarrier, Rx, latex free, sterile, Qty 1, Zimmer, Dover, Ohio; REF 00-2195-015-00. Single use device for use during skin grafting procedures.

FDA Recall
Terminated ·Zimmer Inc.·Product code FZW·April 3, 2008

Zimmer Dermacarriers skin graft carriers, S.G. Carrier 8IN length, Rx, latex free, sterile, Zimmer, Dover, Ohio; REF 00-7708-000-10. Single use device for use during skin grafting procedures.

FDA Recall
Terminated ·Zimmer Inc.·Product code FZW·April 3, 2008

Zimmer Dermacarriers Skin Graft Carriers, S.G. Carrier 16IN length, Rx, latex free, sterile, Zimmer, Dover, Ohio; REF 00-7716-000-10. Single use device for use during skin grafting procedures.

FDA Recall
Terminated ·Zimmer Inc.·Product code FZW·April 3, 2008

Zimmer Dermacarriers II skin graft carriers, 3 to 1 dermacarrier, Rx, latex free, sterile, Qty 1, Zimmer, Dover, Ohio; REF 00-2195-013-00. Single use device for use during skin grafting procedures.

FDA Recall
Terminated ·Zimmer Inc.·Product code FZW·April 3, 2008

Zimmer Dermacarriers II skin graft carriers, 1.5 to 1 dermacarrier, Rx, latex free, sterile, Zimmer, Dover, Ohio; REF 00-2195-012-00. Single use device for use during skin grafting procedures.

FDA Recall
Terminated ·Zimmer Inc.·Product code FZW·April 3, 2008

Brennen Skin Graft Mesher. Surgical instrument designed to expand skin grafts'

FDA Recall
Open, Classified ·Molnlycke Health Care, Inc·Product code FZW·April 24, 2017

Zimmer Dermacarriers II skin graft carriers, 6 to 1 dermacarrier, Rx, latex free, sterile, Qty 1, Zimmer, Dover, Ohio; REF 00-2195-014-00. Single use device for use during skin grafting procedures.

FDA Recall
Terminated ·Zimmer Inc.·Product code FZW·April 3, 2008

MESHGRAFT II

FDA Adverse Event
Injury ·ZIMMER SURGICAL, INC.·Product code FZW·December 16, 2016

ZIMMER SKIN GRAFT MESHER

FDA Adverse Event
Injury ·ZIMMER SURGICAL, INC.·Product code FZW·October 6, 2016

SKIN GRAFT MESHER PLS 02

FDA Adverse Event
Malfunction ·Product code FZW·September 3, 2015

ZIMMER SKIN GRAFT MESHER

FDA Adverse Event
Injury ·ZIMMER BIOMET SURGICAL·Product code FZW·August 12, 2015

ZIMMER SKIN GRAFT MESHER

FDA Adverse Event
Injury ·ZIMMER SURGICAL·Product code FZW·July 9, 2015

ZIMMER SKIN GRAFT MESHER

FDA Adverse Event
Injury ·ZIMMER SURGICAL·Product code FZW·February 6, 2012

ZIMMER SKIN GRAFT MESHER

FDA Adverse Event
Injury ·ZIMMER SURGICAL·Product code FZW·February 6, 2012

ZIMMER SKIN GRAFT MESHER

FDA Adverse Event
Injury ·ZIMMER SURGICAL·Product code FZW·January 4, 2012

ZIMMER SKIN GRAFT MESHER

FDA Adverse Event
Malfunction ·ZIMMER SURGICAL·Product code FZW·March 21, 2012

ZIMMER SKIN GRAFT MESHER

FDA Adverse Event
Malfunction ·ZIMMER SURGICAL·Product code FZW·May 14, 2014