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Musculoskeletal Transplant Foundation, Inc. recalls DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous defect
Recalled November 29, 2023 · FDA recall Z-0323-2024 · Musculoskeletal Transplant Foundation
Hazard
Units are labeled as 10cc; however the units have a fill volume of 1cc units. This may result in prolongation of surgery. · FDA Class II
Units
18 units
Sold at
US Nationwide distribution in the states of PA, TX, WA.
Description
Units are labeled as 10cc; however the units have a fill volume of 1cc units. This may result in prolongation of surgery.
Product
DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous defects created from traumatic injury. Model Number: 038100
Manufacturer(s)
Musculoskeletal Transplant Foundation, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →