[Recalled] RKN130003, RHEO KNEE 3 YR WARRANTY, MD, CE, External lower limb prosthetic component — Due to firmware issues with the prosthetic knee, there is the potential for uni… | FDA 2024-03-25
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | RKN130003, RHEO KNEE 3 YR WARRANTY, MD, CE, External lower limb prosthetic component |
|---|---|
| Brand / manufacturer | Ossur H / F |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1788-2024 |
| Country of notice | Iceland |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 25 March 2024 |
| EAN / barcode | 05690967595418 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Due to firmware issues with the prosthetic knee, there is the potential for unintended warnings and device shutdown which could result in patient falls.
This Class II recall concerns device products distributed in Iceland 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 Ossur H / F
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.
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