Device recall
Z-2098-2017: SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for the folding…
FDA device recall · Class II · Bausch & Lomb Surgical, Inc.
Key facts
| Recall number (Z-number) | Z-2098-2017 |
|---|---|
| Recall event | 77087 |
| Product | SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for the folding and delivering of the LI61AO, LI61AOV, or LI61SE 3-piece lens into the eye. The SofPort Easy-Load Lens Delivery System consists of a syringe shaped body and tip with a plunger, drawer, and haptic puller. It is a sterile… |
| Product code | MSS |
| Recalling firm | Bausch & Lomb Surgical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 11, 2019 |
| 510(k) numbers | K970727 |
| FEI number | 1119279 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database