Device recall

Z-1688-2022: VYGON DRESSING CHANGE W/MAXISWAB kit, REF AMS-8465CS

FDA device recall · Class II · Stradis Healthcare

Key facts

Recall number (Z-number) Z-1688-2022
Recall event 90693
Product VYGON DRESSING CHANGE W/MAXISWAB kit, REF AMS-8465CS
Product code OXQ
Recalling firm Stradis Healthcare
Recall class Class II
Status Open, Classified
FEI number 1450943

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)