WATCHDOG Hemostasis Valve Kit — Class II medical device recall Z-1592-2023
Ongoing recall by Boston Scientific Corporation, reported 2023-05-24. The firm received complaints of the Insertion Tool component being occluded, resulting in the inability to pas
| Recall number | Z-1592-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Boston Scientific Corporation, Maple Grove, MN, United States |
| Recall initiated | 2023-04-05 |
| Classified | 2023-05-16 |
| Reported by FDA | 2023-05-24 |
| Quantity | 1,300 units |
| UPC / GTIN / UDI-DI | 08714729965794, 08714729996019 |
| Lot numbers | 30272850, 30542947, 30661041, 30845826, 30935565 |
Product
WATCHDOG Hemostasis Valve Kit, UPN H74939343A022 (outer package), UPN H74939343A020 (inner package)
Reason for recall
The firm received complaints of the Insertion Tool component being occluded, resulting in the inability to pass a guidewire through the tool.
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-1592-2023. 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.