GRAFTON PLUS™ DBM T45005INTRecalls & reported problems
Medtronic Sofamor Danek, Inc. · DBM T45005INT 5CC PASTE GRAFTON PLUS · Class 2 · Implant
All models of GRAFTON PLUS DBM (2)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
14 other recalls cover devices cleared under the same FDA submission (K042707, K043048); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- Feb 8, 2023Class IIOpen, Classified
Potential for packaging non-conformances directly related to the dual-barrier, sterile pouch packaging system. Non-conforming packaging may lead to a breach in the sterile barrier.
Z-1329-2023 · Root cause: Process control · Recall details · FDA record ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K042707, K043048. One submission often covers many models, so check the product and lot details in each record.
- Z-0137-2027 · Aug 12, 2026 · Open, ClassifiedGrafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined with an inert additive to yield a demineralized bone matrix (DBM) allograft product having a p
- Z-0166-2024 · Sep 26, 2023 · Open, ClassifiedGrafton Plus DBM Paste, Model Numbers: a) T45001, b) T45005, c) T45010; Demineralized Bone Matrix
- Z-0088-2013 · Apr 20, 2012 · TerminatedGrafton DBM Matrix PLF Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bo
- Z-0091-2013 · Apr 20, 2012 · TerminatedGrafton DBM Orthoblend Large Defect Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a de
- Z-0085-2013 · Apr 20, 2012 · TerminatedGrafton DBM Flex Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone mat
- Z-0093-2013 · Apr 20, 2012 · TerminatedOptimum Expanse R Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allo
- Z-0092-2013 · Apr 20, 2012 · TerminatedGrafton DBM Orthoblend Large Defect Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a de
- Z-0087-2013 · Apr 20, 2012 · TerminatedGrafton DBM Crunch Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone m
- Z-0086-2013 · Apr 20, 2012 · TerminatedGrafton DBM A-Flex Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone m
- Z-0083-2013 · Apr 20, 2012 · TerminatedGrafton DBM Putty Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone ma
- Z-0094-2013 · Apr 20, 2012 · TerminatedOptimum Expanse S Multiple sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone ma
- Z-0084-2013 · Apr 20, 2012 · TerminatedGrafton DBM Gel Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matr
- Z-0089-2013 · Apr 20, 2012 · TerminatedGrafton DBM Matrix Strips Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized
- Z-0090-2013 · Apr 20, 2012 · TerminatedGrafton DBM Orthoblend Small Defect Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a dem
Other Filler, bone void, osteoinduction (w/o human growth factor) devices
- GRAFTON®and GRAFTON PLUS®Demineralized Bone Matrix (DBM) T45005Medtronic Sofamor Danek, Inc. · Filler, bone void, osteoinduction (w/o human growth factor)3 recalls0 reports
- GRAFTON®and GRAFTON PLUS®Demineralized Bone Matrix (DBM) T45010Medtronic Sofamor Danek, Inc. · Filler, bone void, osteoinduction (w/o human growth factor)2 recalls2 reports
- GRAFTON®and GRAFTON PLUS®Demineralized Bone Matrix (DBM) T44135Medtronic Sofamor Danek, Inc. · Filler, bone void, osteoinduction (w/o human growth factor)2 recalls1 report
- GRAFTON®and GRAFTON PLUS®Demineralized Bone Matrix (DBM) T44115Medtronic Sofamor Danek, Inc. · Filler, bone void, osteoinduction (w/o human growth factor)2 recalls1 report
- GRAFTON®and GRAFTON PLUS®Demineralized Bone Matrix (DBM) T45001Medtronic Sofamor Danek, Inc. · Filler, bone void, osteoinduction (w/o human growth factor)2 recalls0 reports
- GRAFTON®and GRAFTON PLUS®Demineralized Bone Matrix (DBM) T42100Medtronic Sofamor Danek, Inc. · Filler, bone void, osteoinduction (w/o human growth factor)2 recalls0 reports
- GRAFTON®and GRAFTON PLUS®Demineralized Bone Matrix (DBM) T42210Medtronic Sofamor Danek, Inc. · Filler, bone void, osteoinduction (w/o human growth factor)2 recalls0 reports
- GRAFTON®and GRAFTON PLUS®Demineralized Bone Matrix (DBM) T43105Medtronic Sofamor Danek, Inc. · Filler, bone void, osteoinduction (w/o human growth factor)1 recall4 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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