Karl Storz Endoscopy America Inc: Medical Device Recall in 2013 - (Recall #: Z-0465-2014)

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:

Axillent Debakey Grasping Forceps, Part No. 33821DYD In general the surgeons use 33821DYD Debakey forceps to grasp tissue.

Product Classification:

Class II

Date Initiated: November 6, 2013

Date Posted: December 18, 2013

Recall Number: Z-0465-2014

Event ID: 66823

Reason for Recall:

KARL STORZ is recalling the Axillent Debakey Grasping Forceps because the 33821WTD Wavy grasper was mislabeled as 33821DYD Axillent Debakey Grasping Forceps.

Status: Terminated

Product Quantity: 7 units

Code Information:

Lot Code YX

Distribution Pattern:

Nationwide Distribution including states of: TX, PA, and NY.

Voluntary or Mandated:

Voluntary: Firm initiated