FDA Device recall Z-2741-2017
MAKO RIO Standard System, internal cPCI Card CageP/N: 201337
- FDA Device
- Class II
- terminated
- Published 2017-07-26
On 2017-07-26 the FDA classified a Class II recall of MAKO RIO Standard System, internal cPCI Card CageP/N: 201337 by Mako Surgical, citing an intermittent electrical problem that could lead to a loss of system power due to a loose screw connection.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2741-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-06-07 |
| Published | 2017-07-26 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Mako Surgical |
| Distribution | AZ, CA, CO, CT, FL, GA, ID, LA, MA, MO, MS, NC, OH, PA, TN, TX, WA |
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
An intermittent electrical problem that could lead to a loss of system power due to a loose screw connection.
Identifiers
| code_info | Lot No. 05212015 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2741-2017%22
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