Recall Z-1240-06 ยท DQO Catheter, Intravascular, Diagnostic
Cordis Corporation
Cordis INFINITI 6 French Diagnostic Catheter. Catalog 534-6xxT. That is: 534614T, 534615T, 534617T, 534618T, 534619T, 534620T, 534621T, 534622T, 534623T, 534624T, 534625T, 534627T, 534628T, 534629T, 534635T, 534637T, 534641T, 534642T, 534643T, 534644T, 534645T, 534646T, 534647T, 534648T, 534649T, 534660T, 534670T, 534672T, 534674T.
| Date | Jul 13, 2006 (initiated Jun 26, 2006) |
| Status | Terminated |
| Reason | The tip of the catheter may separate from the body during operation. |
| Root cause | Other |
| Action | The firm sent a letter in June 2006 to its consignees advising them that all impacted lots of Infiniti 6 French catheters (product codes attached) manufactured on Line #1 from July 2005 through February 2006 are being recalled, starting June 26, 2006. The U.S. initial consignee is being contacted directly by Cordis sales reps and other Cordis representatives. The initial consignee is being requested to sign an Acknowledgement Form. The Cordis representative is collecting any units at the consignee, and sending the units back to Cordis for reconciliation and destruction. |
| Quantity | 338,270 |
| Distribution | Worldwide. |
| FDA record | Open on fda.gov |