AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM — Class II medical device recall Z-0187-2024
Ongoing recall by MICROVENTION INC., reported 2023-11-08, distributed nationwide. Peripheral coil system detachable has a potential of unsealed pouch packaging.
| Recall number | Z-0187-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MICROVENTION INC., Aliso Viejo, CA, United States |
| Recall initiated | 2023-08-24 |
| Classified | 2023-10-27 |
| Reported by FDA | 2023-11-08 |
| Distributed | Nationwide (US) |
| Quantity | 14 |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 00812636021089 |
| Lot numbers | 0000190693 |
| Model numbers | 45-751324 |
| Expiration dates | 2027-04-30 |
Product
AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM, REF: 45-751324
Reason for recall
Peripheral coil system detachable has a potential of unsealed pouch packaging.
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-0187-2024. 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.