Filler, Bone Void, Osteoinduction (w/o Human Growth Factor)
Osteotech, Inc.'s record for this product code
Recent MDR events
49 adverse event reports on file
- GRAFTON DBMOct 11, 2022InjuryMW5112525
- GRAFTON DBMJul 3, 2015Injury2246640-2015-00007
- GRAFTON DBMJul 14, 2014Injury2246640-2014-00008
- NOT REPORTEDJun 11, 2014Injury2246640-2014-00007
- GRAFTON DBMJun 5, 2014Injury2246640-2014-00006
- GRAFTON DBMMay 29, 2014Injury2246640-2014-00005
- GRAFTON DBMMay 22, 2014Injury2246640-2014-00004
- GRAFTON DBMDec 20, 20132246640-2013-00030
- GRAFTON DBMDec 4, 20132246640-2013-00028
- GRAFTON DBM MATRIX PLFNov 19, 2013Injury2246640-2013-00025
Recalls
14 recall events for this product code
- TerminatedOct 18, 2012
Multiple lots of GRAFTON and XPANSE , which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
View FDA record ↗ - TerminatedOct 18, 2012
Multiple lots of GRAFTON and XPANSE , which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
View FDA record ↗ - TerminatedOct 18, 2012
Multiple lots of GRAFTON and XPANSE , which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
View FDA record ↗ - TerminatedOct 18, 2012
Multiple lots of GRAFTON and XPANSE , which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
View FDA record ↗ - TerminatedOct 18, 2012
Multiple lots of GRAFTON and XPANSE , which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
View FDA record ↗ - TerminatedOct 18, 2012
Multiple lots of GRAFTON and XPANSE , which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
View FDA record ↗ - TerminatedOct 18, 2012
Multiple lots of GRAFTON and XPANSE , which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
View FDA record ↗ - TerminatedOct 18, 2012
Multiple lots of GRAFTON and XPANSE , which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
View FDA record ↗ - TerminatedOct 18, 2012
Multiple lots of GRAFTON and XPANSE , which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
View FDA record ↗ - TerminatedOct 18, 2012
Multiple lots of GRAFTON and XPANSE , which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
View FDA record ↗
510(k) clearances
4 clearances for this product code