Device recall

Z-1562-2021: AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for treatment of…

FDA device recall · Class II · Musculoskeletal Transplant Foundation, Inc.

Key facts

Recall number (Z-number) Z-1562-2021
Recall event 87677
Product AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for treatment of surgically-created osseous defects or osseous defects created from traumatic injury. It can be used in the: extremities, pelvis, and spine Item Number: 227007
Product code MQV
Recalling firm Musculoskeletal Transplant Foundation, Inc.
Recall class Class II
Status Terminated
Termination date Apr 27, 2023
FEI number 3001236616

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 100–999 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

Browse all FDA device recalls (products)