[Recalled] Synthes Torque Limiting Handle, Part Number 03.231.013 This device is used in systems indicated for fracture fixation. — The adapter may demonstrate a degradation of function as the final products wer… | FDA 2018-05-04
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | Synthes Torque Limiting Handle, Part Number 03.231.013 This device is used in systems indicated for fracture fixation. |
|---|---|
| Brand / manufacturer | Synthes (USA) Products LLC |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1916-2018 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 04 May 2018 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The adapter may demonstrate a degradation of function as the final products were assembled with ball bearings of high carbon content that is likely to rust prematurely.
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 Synthes (USA) Products LLC
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.