Device recall

Z-1311-2021: Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and…

FDA device recall · Class II · Hollister Incorporated

Key facts

Recall number (Z-number) Z-1311-2021
Recall event 87351
Product Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and accessories) - Product Usage: designed to stabilize and secure a variety of catheters, surgical drains, and tubes from sizes 5-40 French.
Product code KNT
Recalling firm Hollister Incorporated
Recall class Class II
Status Terminated
Termination date Sep 14, 2022
510(k) numbers K932855
FEI number 1480288

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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