Karl Storz Endoscopy: Medical Device Recall in 2019 - (Recall #: Z-2447-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Flexible Intubation Fiberscope, Model # 11301AB1

Product Classification:

Class II

Date Initiated: April 24, 2019

Date Posted: September 11, 2019

Recall Number: Z-2447-2019

Event ID: 83419

Reason for Recall:

The action is being initiated due to intubation scopes improperly manufactured with a double port luer instead of a single port luer.

Status: Terminated

Product Quantity: 14 scopes

Code Information:

Lot numbers: 2183827, 2195794, 2215741, 2229258, 2235373, 2248169, 2193769

Distribution Pattern:

US: VA, MO, CA, OH, NM, NY, CO, LA, ME, OUS: Canada

Voluntary or Mandated:

Voluntary: Firm initiated