Device recall

Z-0615-2021: RevMedX Trauma Dressings are packaged in a Tyvek Peel pouch, 1 Trauma Dressing…

FDA device recall · Class II · Medline Industries Inc

Key facts

Recall number (Z-number) Z-0615-2021
Recall event 86764
Product RevMedX Trauma Dressings are packaged in a Tyvek Peel pouch, 1 Trauma Dressing per Tyvec Peel Pouch, 30 Pouches per Case; Sterile - Product Usage: are intended to absorb exudates.
Product code NAB
Recalling firm Medline Industries Inc
Recall class Class II
Status Terminated
Termination date Aug 4, 2021
FEI number 1417592

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

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