Hemostasis Probe — Class II medical device recall Z-1481-2024
Ongoing recall by Olympus Corporation of the Americas, reported 2024-04-17. The BICOAG Hemostasis Probe with a coaxial plug was mispackaged into the package and labeled as a BICOAG Hemos
| Recall number | Z-1481-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Olympus Corporation of the Americas, Center Valley, PA, United States |
| Recall initiated | 2024-01-05 |
| Classified | 2024-04-05 |
| Reported by FDA | 2024-04-17 |
| Quantity | 36 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00821925039452 |
| Lot numbers | KR214212 |
| Model numbers | CD-B622LA |
Product
Hemostasis Probe, Model: CD-B622LA
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1481-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.