5,562 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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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