Device recall

Z-0492-2015: Ethicon PERMA-HAND Silk siliconized black braided 10 strands per packet Ethicon…

FDA device recall · Class II · Ethicon, Inc.

Key facts

Recall number (Z-number) Z-0492-2015
Recall event 69787
Product Ethicon PERMA-HAND Silk siliconized black braided 10 strands per packet Ethicon LLC- Made in USA.
Product code GAP
Recalling firm Ethicon, Inc.
Recall class Class II
Status Terminated
Termination date Aug 14, 2015
510(k) numbers K946173
FEI number 2210968

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 Products in the same recall event
  • 10–99 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)