[Recalled] MAKO RIO Standard System, internal cPCI Card CageP/N: 201337. Intended to assist the surgeon in providing software defined spatial boundaries during orthopedic procedures. — An intermittent electrical problem that could lead t
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| 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. |
|---|---|
| Brand / manufacturer | Mako Surgical Corporation |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2741-2017 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 07 June 2017 |
| EAN / barcode | 05212015 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: An intermittent electrical problem that could lead to a loss of system power due to a loose screw connection.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Mako Surgical Corporation
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.