Device recall

Z-1425-2023: FLEX. GRASP. FORCEPS 6.6FR WL 550MM, Product Number 8736.685

FDA device recall · Class II · Richard Wolf GmbH

Key facts

Recall number (Z-number) Z-1425-2023
Recall event 91953
Product FLEX. GRASP. FORCEPS 6.6FR WL 550MM, Product Number 8736.685
Product code FCL
Recalling firm Richard Wolf GmbH
Recall class Class II
Status Open, Classified
FEI number 3002808001

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)