Class II

Medical Device Recall: Hemostasis Probe, Model: CD-B622LA

Olympus Corporation of the Americas · January 5, 2024

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.

Distribution

International distribution only.

Quantity Affected

36 units (all OUS)

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1481-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Olympus Corporation of the Americas Medical Device Recall: Hemostasis Probe, Model: CD-B622LA | SafeCheck