Wingman 35 Crossing Catheter — Class I medical device recall Z-1898-2017
Terminated recall by ReFlow Medical, reported 2017-05-24, distributed nationwide. ReFlow Medical is recalling the Wingman 35 Crossing Catheter because it may be prone to tip detachment.
| Recall number | Z-1898-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ReFlow Medical, San Clemente, CA, United States |
| Recall initiated | 2017-03-22 |
| Classified | 2017-05-12 |
| Reported by FDA | 2017-05-24 |
| Terminated | 2017-12-06 |
| Distributed | Nationwide (US) |
| Countries outside the US | DE, TR |
| Quantity | 2,794 units |
| Reason classes | device malfunction |
| Model numbers | 1502053, 1502053R, 1503094, 1503094R, 1503094R1, 1503094R2, 1505061, 1505061R, 1505144, 1505144R, 1505144R1, 1505144R2, 1505144R3, 1505264, 1506104, 1506104R, 1508074, 1508074R, 1508204, 1508204R, 1508205, 1508205R, 1508264, 1508264R, 1508265 and 55 more |
Product
Wingman 35 Crossing Catheter, 65cm, Model Numbers: WGM35065US WGM35065CE WGM35090US WGM35090CE WGM35135US WGM35135CE
Reason for recall
ReFlow Medical is recalling the Wingman 35 Crossing Catheter because it may be prone to tip detachment.
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-1898-2017. 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.