Karl Storz Endoscopy: Medical Device Recall in 2019 - (Recall #: Z-2425-2019)

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 NEURO-FIBERSCOPE, 3.7MM X 34CM, Model # 11282BN1

Product Classification:

Class II

Date Initiated: February 20, 2019

Date Posted: September 4, 2019

Recall Number: Z-2425-2019

Event ID: 83459

Reason for Recall:

The action is being initiated due to Flexible Neuroscopes manufactured with the incorrect channel port.

Status: Terminated

Product Quantity: 22 scopes

Code Information:

SERIAL NUMBER: 2161516, 2204079, 2172240, 2198276, 2062041, 2178784, 2198341, 2220959, 2210200, 2183837, 2188370, 2247464, 2248783, 2194154, 2244117, 2039298

Distribution Pattern:

US: FL, MO, MA, AL,CA, OH, PA,NH, OR, WA, MI, NC, CA, VA

Voluntary or Mandated:

Voluntary: Firm initiated