Stryker Corporation: Medical Device Recall in 2020 - (Recall #: Z-1148-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Stryker, Omega 4.75 mm,. PEEK Knotless Anchor System, Single, REF 3910-500-471, UDI 07613327464818, Sterile R, RX Only CE 0197

Product Classification:

Class II

Date Initiated: July 19, 2019

Date Posted: February 19, 2020

Recall Number: Z-1148-2020

Event ID: 84664

Reason for Recall:

Complaints have been received regarding difficulty in removing the driver from the screw. High driver removal forces can lead to the screw pulling out still attached to the driver. This could result in an additional anchor insertion site in the bone being used.

Status: Terminated

Product Quantity: 87 devices

Code Information:

19113AG2, 19130AG2, 19134AG2, 19115AG2, 19131AG2, 19133AG2, 19154AG2,19155AG2, 19156AG2, 19157AG2, 19149AG2.

Distribution Pattern:

US: GA, NJ, NY, KY, MD, TX, UT, AZ, IL, ID, CO, OH, FL, AK, CA, NV, AR, ME, WI

Voluntary or Mandated:

Voluntary: Firm initiated