Karl Storz Endoscopy America Inc: Medical Device Recall in 2013 - (Recall #: Z-1313-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Loop, Cutting, 24FR (26050G/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives).

Product Classification:

Class II

Date Initiated: June 1, 2009

Date Posted: May 22, 2013

Recall Number: Z-1313-2013

Event ID: 55358

Reason for Recall:

Possible damage to the sterile packaging (blister tray) of some Karl Storz sterile products, which may result in airborne contamination.

Status: Terminated

Product Quantity: 9432 units

Code Information:

Lot 36781

Distribution Pattern:

Distributed Nationwide and in Canada.

Voluntary or Mandated:

Voluntary: Firm initiated