Olympus Corporation of the Americas: Medical Device Recall in 2024 - (Recall #: Z-1213-2024)

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 PCF-HQ190L.

Product Classification:

Class II

Date Initiated: January 11, 2024

Date Posted: March 6, 2024

Recall Number: Z-1213-2024

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: 28

Code Information:

Model Number: PCF-HQ190L; UDI DI: 4953170416118; Serial Number: 2000569, 2001007, 2101185, 2101301, 2101313, 2101860, 2102339, 2102634, 2102740, 2103215, 2103257, 2103483, 2103614, 2103674, 2203899, 2203915, 2204096, 2204400, 2204659, 2204820, 2205238, 2205684, 2206065, 2206501, 2307200, 2307709, 2307713, 2308226;

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated