FDA Device recall Z-1557-2022
Echelon -14 Micro Catheter, REF: 105-5092-150, sterile EO, Rx Only
- FDA Device
- Class II
- ongoing
- Published 2022-08-24
On 2022-08-24 the FDA classified a Class II recall of Echelon -14 Micro Catheter, REF: 105-5092-150, sterile EO, Rx Only by Micro Therapeutics, citing outer carton packaging of microcatheters were exposed to wet substance during transport.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1557-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-06-30 |
| Published | 2022-08-24 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Micro Therapeutics |
| Distribution | US |
Product
Echelon -14 Micro Catheter, REF: 105-5092-150, sterile EO, Rx Only
Reason
Outer carton packaging of microcatheters were exposed to wet substance during transport.
Identifiers
| code_info | Lot # B262322 UDI: (00) 847536005983 |
|---|
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-1557-2022%22
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