Musculoskeletal Transplant Foundation, Inc. QuickGraft Model # 430PST Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
QuickGraft Model # 430PST
Brand
Musculoskeletal Transplant Foundation, Inc.
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Serial # 00319004921075 00319004921073 00319007681048 00319014411085 00618052231059 03319006511040 03319009191029 03319019231072 03519018121056
Musculoskeletal Transplant Foundation, Inc. is recalling QuickGraft Model # 430PST due to Measurement listed on the label is not taken under tension, and this would cause possible extension of surgical time needed to complete the procedure.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Measurement listed on the label is not taken under tension, and this would cause possible extension of surgical time needed to complete the procedure.
Recommended Action
Per FDA guidance
You may choose to add the additional label to the unit(s), this may be completed by an appropriate Sales Representative or hospital staff. Or, you may choose to have the unit(s) returned to MTF for the labelling correction
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
LA, MO, NY, NC, OH, TX
Page updated: Jan 10, 2026