XTANT MEDICAL INC: Medical Device Recalls in 2020

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by XTANT MEDICAL INC in 2020. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

OsteoSelect Demineralized Bone Matrix (DBM) Putty 10.0cc in a syringe; STERILE R, Product Code: 359100, Dimensions: ONE(1) PACKAGE - CONTAINING 10.0cc. UDI: 00849777003681 - Product Usage: OsteoSelect DBM Putty is indicated for use as a bone void filler and bone graft substitute for voids or gaps that are not intrinsic to the stability of the bony structure. OsteoSelect DBM Putty is indicated for treatment of surgically created osseous defects or osseous defects from traumatic injury to the bone. OsteoSelect DBM Putty can be used as follows: - Extremities - Posterolateral spine - Pelvis.