Olympus Corporation of the Americas: Medical Device Recall in 2024 - (Recall #: Z-1206-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Colonoscope, Model Number CF-HQ190I.

Product Classification:

Class II

Date Initiated: January 11, 2024

Date Posted: March 6, 2024

Recall Number: Z-1206-2024

Event ID: 93832

Reason for Recall:

Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration, fluctuation in temperature or severe shock loads.

Status: Ongoing

Product Quantity: 1

Code Information:

Model Number: CF-HQ190I; UDI DI: 4953170305139; Serial Number: 2263354;

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated