Home / Recalls / Musculoskeletal Transplant Foundation, Inc. / Z-2548-2019

Z-2548-2019 Class II Terminated

Recalled by Musculoskeletal Transplant Foundation, Inc. — Edison, NJ

Recall Details

Product Type
Devices
Report Date
October 2, 2019
Initiation Date
August 15, 2019
Termination Date
July 1, 2020
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
9 Qty

Product Description

QuickGraft¿ Model # 430PST

Reason for Recall

Measurement listed on the label is not taken under tension, and this would cause possible extension of surgical time needed to complete the procedure.

Distribution Pattern

NY NC LA TX MO OH

Code Information

Serial # 00319004921075 00319004921073 00319007681048 00319014411085 00618052231059 03319006511040 03319009191029 03319019231072 03519018121056

Other recalls by Musculoskeletal Transplant Foundation, Inc.

  • Z-1066-2024 Class II — AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bon (December 22, 2023)
  • Z-1067-2024 Class II — AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bon (December 22, 2023)
  • Z-0323-2024 Class II — DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically c (September 22, 2023)
  • Z-1562-2021 Class II — AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for treatment of surgica (March 29, 2021)
  • Z-2004-2016 Class II — Musculoskeletal Transplant Foundation, AFT Diverted Tube (3/4/Filled), indicated (April 21, 2016)
  • Z-2210-2015 Class II — Cortical Pin 2.0 mm,Sterile, FREEZE DRIED: Store at ambient temperature. Do Not (May 27, 2015)
  • Z-2075-2015 Class II — Allofix Insertion Kit, 2.0 mm, Single Drill, Product Usage: MTF Surgical In (May 27, 2015)
  • Z-1455-2015 Class II — DBX Mix, 20 cc, Product Code: 058200. Demineralized Bone Matrix Mix, bone void (December 4, 2014)