Olympus Corporation of the Americas: Medical Device Recall in 2024 - (Recall #: Z-1481-2024)

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:

Hemostasis Probe, Model: CD-B622LA

Product Classification:

Class II

Date Initiated: January 5, 2024

Date Posted: April 17, 2024

Recall Number: Z-1481-2024

Event ID: 94150

Reason for Recall:

The BICOAG Hemostasis Probe with a coaxial plug was mispackaged into the package and labeled as a BICOAG Hemostasis Probe with a fixed pin connector.

Status: Ongoing

Product Quantity: 36 units (all OUS)

Code Information:

Model Number: CD-B622LA; UDI/DI: 00821925039452; Lot Number: KR214212

Distribution Pattern:

International distribution only.

Voluntary or Mandated:

Voluntary: Firm initiated