[Recalled] Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229003A Model: VST66DF AIM — Potential that the coating of the light head forks on the VOLISTA Surgical Ligh… | FDA 2019-05-28
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229003A Model: VST66DF AIM |
|---|---|
| Brand / manufacturer | Maquet Cardiovascular Us Sales, Llc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1860-2019 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 28 May 2019 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Potential that the coating of the light head forks on the VOLISTA Surgical Lights may crack, posing the risk of particles falling into the surgical field during surgery that may result in patient infection
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 Maquet Cardiovascular Us Sales, 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.