ClearanceBrief
Recall Z-0166-2024 ยท MBP Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)

Medtronic Sofamor Danek USA Inc

Grafton Plus DBM Paste, Model Numbers: a) T45001, b) T45005, c) T45010; Demineralized Bone Matrix

DateOct 25, 2023 (initiated Sep 26, 2023)
StatusOpen, Classified
ReasonSpecific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed according to requirements. Based on this, batches may have been released with potential non-conformances in the outer Tyvek pouch.
Root causeEmployee error
ActionMedtronic issued an URGENT: MEDICAL PRODUCT RECALL notice to its consignees on 09/26/2023 via UPS 2-day delivery. The notice explained the problem, potential risk, and requested the return of the affected devices.
Quantity583 units
DistributionUS, Colombia, S. Korea, New Zealand, India, Taiwan
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K043048GRAFTON PLUS DBM PASTE
Osteotech, Inc., Nov 23, 2005
K051195GRAFTON DBM
Osteotech, Inc., Dec 16, 2005