GRAFTON® DBM T42308INTRecalls & reported problems
Medtronic Sofamor Danek, Inc. · DBM T42308INT GRAFTON M PLUGS 8MMX10MM · Class 2 · Implant
All models of GRAFTON DBM (11)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00643169134539), received between Feb 5, 2018 and Feb 5, 2018 — classified as 1 injury.
13 other recalls cover devices cleared under the same FDA submission (K051188); 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 16, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Herpes1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 5, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE PATIENT UNDERWENT DENTAL SURGERY IN WHICH THE BONE GRAFT WAS USED. IT WAS REPORTED THAT POST-OPERATIVELY, THE PATIENT COMPLAINED OF HAVING HERPES 1 AND 2 VIRUS. THE SURGEON IS UNSURE IF THE CAUSE OF THE DISEASE IS THE GRAFT.
Patient problems: Herpes
MAUDE report 7240885 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K051188. One submission often covers many models, so check the product and lot details in each record.
- Z-0977-2014 · Jan 6, 2014 · TerminatedMedtronic GRAFTON (R) DBM, Flex 2.5cm x 10cm, REF T42100, Rx only, STERILE A, QTY: 1 EA, Medtronic Sofamor Danek, USA, Inc., 1800 Pyramid Place, Memphis, TN 38132 Orthopaedic - f
- 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-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-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-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-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
- 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-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-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-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-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-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
Other BONE GRAFTING MATERIAL, HUMAN SOURCE devices
- GRAFTON® DBM T43110INTMedtronic Sofamor Danek, Inc. · BONE GRAFTING MATERIAL, HUMAN SOURCE1 recall2 reports
- GRAFTON® DBM T43102INTMedtronic Sofamor Danek, Inc. · BONE GRAFTING MATERIAL, HUMAN SOURCE1 recall0 reports
- GRAFTON® DBM T43103INTMedtronic Sofamor Danek, Inc. · BONE GRAFTING MATERIAL, HUMAN SOURCE1 recall0 reports
- GRAFTON® DBM T43101INTMedtronic Sofamor Danek, Inc. · BONE GRAFTING MATERIAL, HUMAN SOURCE1 recall0 reports
- GRAFTON® DBM T43105INTMedtronic Sofamor Danek, Inc. · BONE GRAFTING MATERIAL, HUMAN SOURCE1 recall0 reports
- DynaBlast 10.210.1050Keystone Dental, Inc. · BONE GRAFTING MATERIAL, HUMAN SOURCE3 reports
- GRAFTON® DBM T43110INTMedtronic Sofamor Danek, Inc. · BONE GRAFTING MATERIAL, HUMAN SOURCE1 report
- OpteCure 650-00-01Exactech, Inc. · Bone Grafting Material, Human Source1 report
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 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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