Home / Recalls / Stryker Sustainability Solutions / Z-1626-2016

Z-1626-2016 Class II Terminated

Recalled by Stryker Sustainability Solutions — Tempe, AZ

FDA device recall Z-1626-2016 was initiated by Stryker Sustainability Solutions on Apr 4, 2016 and is designated Class II. Reason for recall: Device packaging may not be sealed. The recall status is terminated (terminated Jul 13, 2016). Affected quantity: 2.

Recall Details

Product Type: Devices
Report Date: May 18, 2016
Initiation Date: Apr 4, 2016
Termination Date: Jul 13, 2016
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 2

Product Description

Launcher Guiding Catheter Model #LA6EBU30. Used in the coronary or peripheral vascular system..

Reason for Recall

Device packaging may not be sealed.

Distribution Pattern

US distribution to KY.

Code Information

Lot #481938U

Source

Dataset: openFDA device recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for Z-1626-2016
openFDA file date: Oct 23, 2026
Loaded by RegDataLab: Oct 25, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.