Device recall

Z-2210-2015: Cortical Pin 2.0 mm,Sterile, FREEZE DRIED: Store at ambient temperature. Do Not…

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

Key facts

Recall number (Z-number) Z-2210-2015
Recall event 71564
Product Cortical Pin 2.0 mm,Sterile, FREEZE DRIED: Store at ambient temperature. Do Not freeze.
Product code JDW
Recalling firm Musculoskeletal Transplant Foundation, Inc.
Recall class Class II
Status Terminated
Termination date Dec 17, 2015
510(k) numbers K061498
FEI number 3001236616

At a glance

  • 1–9 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

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