Device recall

Z-0202-2013: "***Sharpoint IQ Geometry Slit Knife Angled, Bevel Up***Surgical Specialties…

FDA device recall · Class II · Surgical Specialties Puerto Rico Inc. dba Angiotech PR Inc.

Key facts

Recall number (Z-number) Z-0202-2013
Recall event 62945
Product "***Sharpoint IQ Geometry Slit Knife Angled, Bevel Up***Surgical Specialties Corporation Reading, PA***REF 72-2840***" Ophthalmic surgery
Product code GES
Recalling firm Surgical Specialties Puerto Rico Inc. dba Angiotech PR Inc.
Recall class Class II
Status Terminated
Termination date Jan 13, 2014
FEI number 3008845715

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)