Device recall

Z-2612-2011: 45cm Laparoscopic Instruments Sterilization tray. Manufactured by: Stryker…

FDA device recall · Class II · Stryker Endoscopy

Key facts

Recall number (Z-number) Z-2612-2011
Recall event 59072
Product 45cm Laparoscopic Instruments Sterilization tray. Manufactured by: Stryker Endoscopy, 5900 Optical Court,San Jose, CA 95138 Designed to hold laparoscopic surgical manual instruments which are intended for cutting, holding, grasping and manipulating tissue, organs, organ area, surgical auxiliaries…
Product code KCT
Recalling firm Stryker Endoscopy
Recall class Class II
Status Terminated
Termination date Oct 25, 2011
510(k) numbers K960738
FEI number 2936485

At a glance

  • 1–9 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

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