Reported Nov 29, 2023 · Ongoing

DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous…

Musculoskeletal Transplant Foundation, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Musculoskeletal Transplant Foundation, Inc. · 125 May St Ste 300 · Edison, NJ · 08837-3264

Is this the product you have?

  • DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous defects created from traumatic injury
  • Model Number038100
Lot codes and dates
  • GUIDW4184038100T0473 Serial #s:
    • 002220854711400006
    • 002220854711400056
    • 002220854711400003
    • 002220854711400008
    • 002220854711400009
    • 002220854711400001
    • 002220854711400002
    • 002220854711400010
    • 002220854711400011
    • 002220854711400012
    • 002220854711400013
    • 002220854711400014
    • 002220854711400004
    • 002220854711400005
    • 002220854711400007
    Exp
  • Date
    • June 20
    • 2025
Amount recalled
18 units

Where it was sold

Why it was recalled

Units are labeled as 10cc; however the units have a fill volume of 1cc units. This may result in prolongation of surgery.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:58 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.