Recall Z-0138-04 ยท DXT Injector And Syringe, Angiographic
Merit Medical Systems, Inc
IntelliSystem25 Inflation Device and Fluid Dispensing Syringe - Label on package reads in part: ''INTELLISYSTEM 25 WITH MAP152 MAP152 CONTAINS: MERIT ACCESS PLUS LARGE BORE HEMOSTASIS VALVE, TORGUE DEVICE AND METAL GUIDE WIRE INSERTION TOOL...MERIT MEDICAL'', Latex free. Sterile if package is unopened or undamaged. Part # 1525/B
| Date | Nov 19, 2003 (initiated Oct 1, 2003) |
| Status | Terminated |
| Reason | There is a potential for the PETG blister trays to bond together with varying degrees of attachment. The potential for non-sterility exists when the attached trays are seperated by force and holes or cracks are generated in the seperated trays. |
| Root cause | Other |
| Action | Merit notified sales representatives, domestic and international accounts and dealers immediately by letter dated October 3, 2003. The manufacturer requests that the use of the affected inventory should immediately cease and that on-hand units should be promptly isolated from general inventory for simultaneous inspection by a site representative and a Merit sales representative. |
| Quantity | 626 units |
| Distribution | Distributed nationwide. International distribution includes Canada, Japan, Korea, England and France. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K884913 | MERIT INTELLIFLATOR(TM) & MERIT MONITOR(TM) Merit Medical Systems, Inc., Apr 18, 1989 |