PlainRecalls
FDA Devices Moderate Class II Terminated

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

Reported: October 3, 2018 Initiated: July 26, 2018 #Z-3240-2018

Product Description

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

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.

Details

Recalling Firm
Stryker GmbH
Units Affected
233
Distribution
Nationwide
Location
Selzach

Frequently Asked Questions

What product was recalled?
Hoffmann LRF Hexapod Software Catalog #: 983031 Software Version #: HLRF 1.0-2/002, HLRF 1.1-2/002. Recalled by Stryker GmbH. Units affected: 233.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 3, 2018. Severity: Moderate. Recall number: Z-3240-2018.