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

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