Device recall

Z-2433-2008: BD Visitec Disposable Instrument (plastic handle) Capsulorhexis Forceps, Sterile…

FDA device recall · Class II · Becton Dickinson and Company

Key facts

Recall number (Z-number) Z-2433-2008
Recall event 49094
Product BD Visitec Disposable Instrument (plastic handle) Capsulorhexis Forceps, Sterile Ref: 581440 Used during cataract and other ophthalmic surgery procedures to grasp lens capsule.
Product code HNR
Recalling firm Becton Dickinson and Company
Recall class Class II
Status Terminated
Termination date Feb 29, 2012
FEI number 1211998

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)