Drug recall
Cordis 5F SUPER TORQUE PIG PIGTAIL SPECIAL, Angiographic Catheter, REF SRD7040MB
FDA recall event 88372 · Class I · Cordis Corporation
Key facts
| Event ID | 88372 |
|---|---|
| Recall numbers | Z-2428-2021, Z-2429-2021, Z-2430-2021, Z-2431-2021, Z-2432-2021 |
| Recalling firm | Cordis Corporation |
| Product type | Devices |
| Products | Cordis 5F SUPER TORQUE PIG PIGTAIL SPECIAL, Angiographic Catheter, REF SRD7040MB, Cordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB, SPECIAL, Angiographic Catheter, REF SRD6785MB, Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598A, Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598B, Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598C |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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… |
| Initiation date | Jul 21, 2021 |
| Report date | Sep 22, 2021 |
| Termination date | Sep 9, 2024 |
| City | Miami Lakes |
| State | FL |
| Country | United States |
| FEI number | 1016427 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: