Device recall

Z-1945-2015: Gentle Threads Interference Screw 9x35mm Full Thread. An interference fixation…

FDA device recall · Class II · Biomet, Inc.

Key facts

Recall number (Z-number) Z-1945-2015
Recall event 71526
Product Gentle Threads Interference Screw 9x35mm Full Thread. An interference fixation screw for use in soft tissue reattachment procedures
Product code HWC
Recalling firm Biomet, Inc.
Recall class Class II
Status Terminated
Termination date Dec 22, 2015
510(k) numbers K982497
FEI number 1825034

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

Browse all FDA device recalls (products)