Stryker Spine: Medical Device Recall in 2016 - (Recall #: Z-0828-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Stryker Aero-AL Impaction handle Catalog Number 48921007. Stryker Spine Manufactured by : Stryker Spine SAS France Used to facilitate insertion of the Aero-AL cage into the disc space.

Product Classification:

Class II

Date Initiated: December 18, 2015

Date Posted: March 2, 2016

Recall Number: Z-0828-2016

Event ID: 73180

Reason for Recall:

Reported jamming of the impaction handle when assembled to the Inserter guide at the threads.

Status: Terminated

Product Quantity: 31 units

Code Information:

Lot #144933, 14D252, and 14D253.

Distribution Pattern:

Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated