Device recall

Z-0534-2015: A zipser clamp is an instrument used to compress reduce blood flow to the penis…

FDA device recall · Class II · Instrumed International, Inc.

Key facts

Recall number (Z-number) Z-0534-2015
Recall event 69471
Product A zipser clamp is an instrument used to compress reduce blood flow to the penis and reduce pain and is sold under the Medline Industries, Boss Instruments, Millennium Surgical, Medetz Surgical, Surgical Direct, and Surgipro brand names.
Product code HFX
Recalling firm Instrumed International, Inc.
Recall class Class II
Status Terminated
Termination date Nov 29, 2017
FEI number 1421101

At a glance

  • None Linked 510(k)s
  • 10–99 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)