Lower riskMedical device recall · FDA · Published September 22, 2023
DBX Bone Putty 10cc Labeled but Only 1cc Filled May Prolong Surgery
Musculoskeletal Transplant Foundation recalls DBX Demineralized Bone Matrix Putty labeled 10cc but actually 1cc. This may prolong surgery. Product model 038100 with specific serial numbers.
“DBX Bone Putty 10cc Labeled but Only 1cc Filled May Prolong Surgery.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/57280-dbx-bone-putty-10cc-labeled-but-only-1cc-filled-may. Based on FDA recall #Z-0323-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0323-2024%22&limit=1).
The FDA announced on September 22, 2023, that Musculoskeletal Transplant Foundation, Inc. is recalling DBX Demineralized Bone Matrix Putty because units labeled as 10cc actually contain only 1cc. This error may result in the prolongation of surgery. The agency issued recall number Z-0323-2024.
The FDA stated that the units are labeled as 10cc but have a fill volume of 1cc. This discrepancy may result in prolongation of surgery.
Context
GovInfoNow's records show Musculoskeletal Transplant Foundation, Inc. has had three other recalls since August 15, 2019. On December 22, 2023, the company recalled AFT bone void filler tubes due to surgery risks related to filling process qualification. On March 29, 2021, the firm recalled AFT Straight Tubes because they were filled only halfway, posing a risk of surgical delay. Other recent recalls of similar products include IsoTis OsteoBallast Spine Implants (July 2, 2026) and Orthorebirth ZENBONE Bone Filler (March 25, 2026).
How to tell if you have this one
Check for model number 038100 and serial numbers listed in the recall notice. The product was sold with an expiration date of June 20, 2025.
Brand
Musculoskeletal Transplant Foundation
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the model number 038100 and serial numbers listed in the recall notice.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 3 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “US Nationwide distribution in the states of PA, TX, WA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Pennsylvania, Texas, Washington.
Recall timeline
FDA published this recall 2 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0323-2024 (September 22, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0323-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.