FDA Device recall Z-1626-2016
Launcher Guiding Catheter Model #LA6EBU30
- FDA Device
- Class II
- terminated
- Published 2016-05-18
On 2016-05-18 the FDA classified a Class II recall of Launcher Guiding Catheter Model #LA6EBU30 by Stryker Sustainability Solutions, citing device packaging may not be sealed.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1626-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-04-04 |
| Published | 2016-05-18 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Stryker Sustainability Solutions |
| Distribution | KY |
Product
Launcher Guiding Catheter Model #LA6EBU30. Used in the coronary or peripheral vascular system..
Reason
Device packaging may not be sealed.
Identifiers
| code_info | Lot #481938U |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1626-2016%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.