Device recall

Z-1667-2011: Innovate Esmark Bandages, a component of various Presource Custom Sterile…

FDA device recall · Class II · Cardinal Health

Key facts

Recall number (Z-number) Z-1667-2011
Recall event 57880
Product Innovate Esmark Bandages, a component of various Presource Custom Sterile Packs/Presource PBDS Modules; Packaged by Cardinal Health Medical Products and services, McGaw Park, IL 60085 U.S.A.; There is no label on the Esmark bandage in the Presource pack/module, Some are placed in Tyvek pouches and…
Product code LRO
Recalling firm Cardinal Health
Recall class Class II
Status Terminated
Termination date Sep 4, 2012
FEI number 3001236905

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 1,000+ 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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