FDA Device recall Z-1481-2024
Hemostasis Probe, Model: CD-B622LA
- FDA Device
- Class II
- ongoing
- Published 2024-04-17
On 2024-04-17 the FDA classified a Class II recall of Hemostasis Probe, Model: CD-B622LA by Olympus, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1481-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-01-05 |
| Published | 2024-04-17 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Olympus |
| Distribution | n/a |
Product
Hemostasis Probe, Model: CD-B622LA
Reason
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.
Identifiers
| code_info | Model Number: CD-B622LA; UDI/DI: 00821925039452; Lot Number: KR214212 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1481-2024%22
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