Echelon -14 — Class II medical device recall Z-1556-2022
Ongoing recall by Micro Therapeutics, Inc., reported 2022-08-24, distributed nationwide. Outer carton packaging of microcatheters were exposed to wet substance during transport.
| Recall number | Z-1556-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Micro Therapeutics, Inc., Irvine, CA, United States |
| Recall initiated | 2022-06-30 |
| Classified | 2022-08-18 |
| Reported by FDA | 2022-08-24 |
| Distributed | Nationwide (US) |
| Countries outside the US | BR |
| Quantity | 8 units |
| UPC / GTIN / UDI-DI | 00847536006270 |
| Lot numbers | B177543 |
| Model numbers | 145-5092150 |
Product
Echelon -14, 45 Tip Shape, REF 145-5092150, sterile EO, Rx Only
Reason for recall
Outer carton packaging of microcatheters were exposed to wet substance during transport.
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-1556-2022. 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.