Stryker GmbH: Medical Device Recall in 2018 - (Recall #: Z-3240-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Hoffmann LRF Hexapod Software Catalog #: 983031 Software Version #: HLRF 1.0-2/002, HLRF 1.1-2/002

Product Classification:

Class II

Date Initiated: July 26, 2018

Date Posted: October 3, 2018

Recall Number: Z-3240-2018

Event ID: 80863

Reason for Recall:

When creating a correction plan with the Correct Axial First button selected and the No. of corrections per day set to more than 1 (e.g., 2, 3, or 4), the Hexapod Software computes an erroneously accelerated correction plan for the axial portion of the plan.

Status: Terminated

Product Quantity: 233

Code Information:

Version #: HLRF 1.0-2/002, HLRF 1.1-2/002

Distribution Pattern:

Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated