Launcher Guiding Catheter Model #LA6EBU30 — Class II medical device recall Z-1626-2016
Terminated recall by Stryker Sustainability Solutions, reported 2016-05-18, distributed in KY. Device packaging may not be sealed.
| Recall number | Z-1626-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Sustainability Solutions, Tempe, AZ, United States |
| Recall initiated | 2016-04-04 |
| Classified | 2016-05-09 |
| Reported by FDA | 2016-05-18 |
| Terminated | 2016-07-13 |
| Distributed | KY |
| Quantity | 2 |
| Lot numbers | 481938U |
| Model numbers | LA6EBU30 |
Product
Launcher Guiding Catheter Model #LA6EBU30. Used in the coronary or peripheral vascular system..
Reason for recall
Device packaging may not be sealed.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1626-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.