Stryker Sustainability Solutions: Medical Device Recall in 2016 - (Recall #: Z-1626-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: April 4, 2016

Date Posted: May 18, 2016

Recall Number: Z-1626-2016

Event ID: 73835

Reason for Recall:

Device packaging may not be sealed.

Status: Terminated

Product Quantity: 2

Code Information:

Lot #481938U

Distribution Pattern:

US distribution to KY.

Voluntary or Mandated:

Voluntary: Firm initiated