Device recall

Z-0900-05: Gold Hub Monty Infiltration Cannula, Catalog Nos. IC14HM20; IC16HM15; IC18HM15…

FDA device recall · Class II · HK Surgical Inc

Key facts

Recall number (Z-number) Z-0900-05
Recall event 31878
Product Gold Hub Monty Infiltration Cannula, Catalog Nos. IC14HM20; IC16HM15; IC18HM15; IC14HM20; IC16HM15; IC18HM15.
Product code FIE
Recalling firm HK Surgical Inc
Recall class Class II
Status Terminated
Termination date Apr 19, 2012
FEI number 1000125732

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 1–9 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)