Device recall

Z-0525-2019: Family Wellness First Aid Sterile Gauze Pad 3 in x 3 in, 10 CT. White, bleached…

FDA device recall · Class II · ASO, LLC

Key facts

Recall number (Z-number) Z-0525-2019
Recall event 81555
Product Family Wellness First Aid Sterile Gauze Pad 3 in x 3 in, 10 CT. White, bleached, non-woven, rayon/polyester sterile Gauze Pad 3 inch x 3 inch, 12-ply 10 count cardboard box
Product code NAB
Recalling firm ASO, LLC
Recall class Class II
Status Open, Classified
FEI number 1038758

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

Browse all FDA device recalls (products)