DEPLOYDatabase

Incident · Recall

Stryker recalls Mako MICS Handpiece (2024) over a characterization error that can cause off-plan bone cuts

Stryker recalled the Mako Integrated Cutting System (MICS) Handpiece over a saw-blade characterization error that could cause bone-preparation discrepancies. Distinct from the 2020 MICS checkpoint-verification recall already recorded. 897 units. Source: FDA Class 2 device recall Z-0044-2025, accessdata.fda.gov / openFDA enforcement.

Occurred 2024-08-07 · Stryker · Investigated by FDA

How to read this record

Incident records on DEPLOY are compiled from public sources (regulatory filings, news reports, and operator disclosures) and reflect what has been reported and tracked to date. They are not legal findings, determinations of fault, or safety ratings, and may be updated as new information is verified. See the sources below for the underlying references.
Track Stryker recalls Mako MICS Handpiece (2024) over a characterization error that can cause off-plan bone cuts

Machine-readable surfaces

Sources (1)

  1. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?start_search=1&firmlegalnam=Stryker&productdescriptiontxt=Mako&postdatefrom=01/01/2017&postdateto=12/31/2026&PAGENUM=100

Common questions

What happened in Stryker recalls Mako MICS Handpiece (2024) over a characterization error that can cause off-plan bone cuts?
Stryker recalled the Mako Integrated Cutting System (MICS) Handpiece over a saw-blade characterization error that could cause bone-preparation discrepancies. Distinct from the 2020 MICS checkpoint-verification recall already recorded. 897 units. Source: FDA Class 2 device recall Z-0044-2025, accessdata.fda.gov / openFDA enforcement.
When did this incident occur?
The incident is recorded as occurring on August 7, 2024 on the DEPLOY registry. The date reflects the underlying real-world event, not the registry record's creation date.
Who was involved in Stryker recalls Mako MICS Handpiece (2024) over a characterization error that can cause off-plan bone cuts?
The incident is recorded as involving Stryker on the DEPLOY registry. No specific robot model is linked to this incident in the registry.
Has anyone responded to Stryker recalls Mako MICS Handpiece (2024) over a characterization error that can cause off-plan bone cuts?
No responses to this incident are recorded on the DEPLOY registry. Operators, manufacturers, or affected parties can submit responses to the editorial team; absence is not a guarantee no response was issued.
What is the current status of Stryker recalls Mako MICS Handpiece (2024) over a characterization error that can cause off-plan bone cuts?
This incident is an active record on the DEPLOY registry; no retraction or correction has been issued.
Methodology: Verified · 1 source (1 primary) · last reviewed 2026-08-09

Verification posture

Verified

High confidence

Review state

Stable

Last reviewed 2026-08-09

Sources by quality tier

1
primary-fda-database
FDA database

The framework is documented at /methodology. Corrections at /corrections. Reviewer: DEPLOY editorial team.

Methodology surface for Stryker recalls Mako MICS Handpiece (2024) over a characterization error that can cause off-plan bone cuts.

Deploy Watch

Track this incident.

We notify you when the regulator updates the record, the remedy status changes, or a related incident surfaces.

Canonical ID 9221069c-05d7-4ab9-bcc1-f8c09235f463