Musculoskeletal Transplant Foundation DBX Demineralized Bone Matrix Putty 10cc-Indicated for recall — FDA Z-0323-2024
Units are labeled as 10cc; however the units have a fill volume of 1cc units. This may result in prolongation of surgery.
Overview of recall records associated with Musculoskeletal Transplant Foundation, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 6.
Units are labeled as 10cc; however the units have a fill volume of 1cc units. This may result in prolongation of surgery.
3/4 AFT Straight Fill Tubes (227007) filled only 1/2 way instead of 3/4, may cause delay of surgery
AFT Diverted Tubes are being recalled due to a customer complaint involving one unit which had an unsealed Tyvek pouch. The non-sterile foil pouch may introduce contamination into the…
Musculoskeletal Transplant Foundation (MTF) is recalling one lot of MTF's Allograft Cortical Pins because the lot was labeled as a 2.0 mm diameter pin and it may contain a 2.4 mm diameter…
Musculoskeletal Transplant Foundation is recalling a certain lot of Allofix Insertion Kits because they are labeled as having a 2.0mm diameter drill however it may contain a 2.4 mm diameter…
The seal on the DBX Mix outer PETG/Aclar tray with foil lid packaging for lot identified above may not be fully intact.
This page summarizes recall records in which the official source identifies Musculoskeletal Transplant Foundation, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.