Cordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB — Class I medical device recall Z-2428-2021
Terminated recall by Cordis Corporation, reported 2021-09-22, distributed nationwide. Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with Marker Bands) are being used in a m
| Recall number | Z-2428-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cordis Corporation, Miami Lakes, FL, United States |
| Recall initiated | 2021-07-21 |
| Classified | 2021-09-15 |
| Reported by FDA | 2021-09-22 |
| Terminated | 2024-09-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 45 units |
| Model numbers | RD6785MB |
Product
Cordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB, SPECIAL, Angiographic Catheter, REF SRD6785MB
Reason for recall
Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with Marker Bands) are being used in a manner that may allow entrapment of the catheter between endovascular devices and the vessel wall, which can lead to marker band movement or dislodgement.
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-2428-2021. 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.