Z-2645-2023 Class II Ongoing

Recalled by Stryker Corporation — San Jose, CA

FDA device recall Z-2645-2023 was initiated by Stryker Corporation on August 23, 2023 and is designated Class II. Reason for recall: Expired Product distributed The recall status is ongoing. Affected quantity: 96 units.

Recall Details

Product Type
Devices
Report Date
October 4, 2023
Initiation Date
August 23, 2023
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
96 units

Product Description

Cinchlock SS Knotless Anchor Inserter, Part Number CAT02462

Reason for Recall

Expired Product distributed

Distribution Pattern

US Nationwide distribution in the states of NY, NC, GA, TN, KY, IL, UT, AZ, NM, CA.

Code Information

Lot # 19175AE2