[Recalled] Bausch + Lomb Stellaris Elite Vision Enhancement System, 20 ga. Posterior Wide-Field Elite Pack, REF SE5420W (containing the Stellaris Elite 20 GA Vit Cutter, Model BL5626), packaged in sterile trays, 6 trays/shipper. — The back
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | Bausch + Lomb Stellaris Elite Vision Enhancement System, 20 ga. Posterior Wide-Field Elite Pack, REF SE5420W (containing the Stellaris Elite 20 GA Vit Cutter, Model BL5626), packaged in sterile trays, 6 trays/shipper. |
|---|---|
| Brand / manufacturer | Bausch & Lomb Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-3267-2018 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 08 August 2018 |
| EAN / barcode | 00757770059522 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The back cap separates from the body of the vitrectomy cutter.
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 →
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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.