Device recall

Z-0615-2009: Esmark Elastic Bandage, 3" x 4 yards, sterile, for single use only, latex free…

FDA device recall · Class II · Cardinal Health

Key facts

Recall number (Z-number) Z-0615-2009
Recall event 50198
Product Esmark Elastic Bandage, 3" x 4 yards, sterile, for single use only, latex free. Distributed by Cardinal Health, McGaw Park, IL 60085-6787. The device is used to promote blood flow from the extremities by compressing the superficial vessels.
Product code FQM
Recalling firm Cardinal Health
Recall class Class II
Status Terminated
Termination date Nov 4, 2009
FEI number 3001236905

At a glance

  • None 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)