Z-0705-2022 Class II Ongoing

Recalled by K2M, Inc — Leesburg, VA

Recall Details

Product Type
Devices
Report Date
March 9, 2022
Initiation Date
January 13, 2022
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
686 Total Devices

Product Description

Everest MI XT Inner Dilator, Catalog Number 5101-90167

Reason for Recall

Stryker received two (2) complaints for units from specific lots of Inner and Outer Dilators not fitting together properly during a surgical procedure. Some dilators from these lots and from other lots were subsequently determined to be affected by a manufacturing nonconformance.

Distribution Pattern

Worldwide distribution - US Nationwide.

Code Information

GTIN: 10888857261204; Lot Numbers: JUJF KFMV KUPG KYYU MDRB NDMK NDMX NXJK