Recall Z-0670-06 ยท MEA Pump, Infusion, Pca
Stryker Instruments Div. of Stryker Corporation
Stryker PainPump1.5 2-Day Infusion Kit; Product number 501-140-000.
| Date | Mar 21, 2006 (initiated Feb 3, 2006) |
| Status | Terminated |
| Reason | The catheter tubing included in the kit may break during removal. |
| Root cause | Other |
| Action | Each consignee was notified of the recall via recall letter dated 2/7/06, which requested that they destroy the affected lots on site. International accounts were notified via email. |
| Distribution | Nationwide, Australia and Canada. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K042405 | PAINPUMP1; PAINPUMP2 Stryker Corp., Oct 14, 2004 |