FDA Device recall Z-2431-2021
Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598B
- FDA Device
- Class I
- terminated
- Published 2021-09-22
On 2021-09-22 the FDA classified a Class I recall of Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598B by Cordis, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2431-2021 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2021-07-21 |
| Published | 2021-09-22 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Cordis |
| Distribution | US |
Product
Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598B
Reason
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.
Identifiers
| code_info | all codes |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2431-2021%22
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