MAKO RIO Standard System — Class II medical device recall Z-2741-2017
Terminated recall by Mako Surgical Corporation, reported 2017-07-26, distributed in AZ, CA, CO, CT, FL, GA, ID, LA…. An intermittent electrical problem that could lead to a loss of system power due to a loose screw connection.
| Recall number | Z-2741-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mako Surgical Corporation, Davie, FL, United States |
| Recall initiated | 2017-06-07 |
| Classified | 2017-07-18 |
| Reported by FDA | 2017-07-26 |
| Terminated | 2020-06-16 |
| Distributed | AZ, CA, CO, CT, FL, GA, ID, LA, MA, MO, MS, NC, OH, PA, TN, TX, WA |
| Quantity | 20 |
| Lot numbers | 05212015 |
Product
MAKO RIO Standard System, internal cPCI Card CageP/N: 201337. Intended to assist the surgeon in providing software defined spatial boundaries during orthopedic procedures.
Reason for recall
An intermittent electrical problem that could lead to a loss of system power due to a loose screw connection.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2741-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.