Recall Z-2645-2023— Stryker Corporation

Name: FDA recall Z-2645-2023
Creator: U.S. Food and Drug Administration
Published: 2023-08-23

Class II · Ongoing

Class II FDA medical device recall by Stryker Corporation, initiated 2023-08-23. It names one FDA 510(k) clearance: K131769. Product: Cinchlock SS Knotless Anchor Inserter, Part Number CAT02462. Reason: Expired Product distributed.

Recalling firm: Stryker Corporation
Classification: Class II
Status: Ongoing
Initiated: 2023-08-23
Firm location: San Jose, CA, United States

510(k) clearances named in this recall

1 on FDA's record

K131769 — CINCHLOCK KNOTLESS SUTURE ANCHOR, NANOTACK SUTURE ANCHOR 1.4MMPivot Medical, Inc.·cleared 2013-10-07

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

Cinchlock SS Knotless Anchor Inserter, Part Number CAT02462

Reason for recall

Expired Product distributed

Data sourced from openFDA. This site is unofficial and independent of the FDA.