FDA Device recall Z-0205-2015
Medtronic Launcher Coronary Guide Catheter
- FDA Device
- Class II
- terminated
- Published 2014-11-19
On 2014-11-19 the FDA classified a Class II recall of Medtronic Launcher Coronary Guide Catheter by Medtronic Vascular, citing two reports have been received on the 6F launcher Guide Catheter lot (Model Number LA6JR40K; lot No 0007244836} for incorrect usable length of the Guide Catheter. It was reported….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0205-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-10-13 |
| Published | 2014-11-19 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Medtronic Vascular |
| Distribution | IA, IL, KS, NC |
Product
Medtronic Launcher Coronary Guide Catheter; MODEL: LA6JR40K
Reason
Two reports have been received on the 6F launcher Guide Catheter lot (Model Number LA6JR40K; lot No 0007244836} for incorrect usable length of the Guide Catheter. It was reported that the catheters had a usable length of 90 cm instead of 55 cm, which was specified on the packaging label. Usable length is defined as the total length of catheter shaft from the distal end of the strain relief to the
Identifiers
| code_info | Lot Number: 0007244836 MODEL: LA6JR40K |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0205-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.