FDA Device recall Z-0187-2024
AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM, REF: 45-751324
- FDA Device
- Class II
- ongoing
- Published 2023-11-08
On 2023-11-08 the FDA classified a Class II recall of AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM, REF: 45-751324 by Microvention, citing peripheral coil system detachable has a potential of unsealed pouch packaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0187-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-08-24 |
| Published | 2023-11-08 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Microvention |
| Distribution | US |
Product
AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM, REF: 45-751324
Reason
Peripheral coil system detachable has a potential of unsealed pouch packaging.
Identifiers
| code_info | UDI-DI: 00812636021089, Lot: 0000190693, Expiration: 4/30/2027 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0187-2024%22
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