Stryker Sustainability Solutions: Medical Device Recall in 2018 - (Recall #: Z-0467-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Stryker Sustainability Solutions LASSO NAV eco Reprocessed Diagnostic EP Catheters designed to obtain electrophysiological mapping of the cardiac structures of the heart.

Product Classification:

Class II

Date Initiated: August 23, 2018

Date Posted: November 21, 2018

Recall Number: Z-0467-2019

Event ID: 81321

Reason for Recall:

Electrophysiology catheters were identified to be item # D134903 and distributed. It was subsequently determined that these catheters are item # D134909, which is not approved for reprocessing.

Status: Terminated

Product Quantity: 2

Code Information:

Item Number Serial Number D134903 2519054 D134903 2534027 Note: Item # D134909 is not approved for reprocessing by Stryker s Sustainability Solutions Division. Therefore, SSS does not create or possess D134909 labeling. SSS did not receive labeling from the manufacturer.

Distribution Pattern:

US: KS OUS: None

Voluntary or Mandated:

Voluntary: Firm initiated