Device recall
Z-0030-2022: Nutrifill Scleral, Hybrid, and Gas Permeable (GP) Lens Insertion Solution…
FDA device recall · Class II · Contamac Solutions, Inc.
Key facts
| Recall number (Z-number) | Z-0030-2022 |
|---|---|
| Recall event | 88529 |
| Product | Nutrifill Scleral, Hybrid, and Gas Permeable (GP) Lens Insertion Solution, Physiologic Formula, Preservative Free, 35 Single-use 10ml ampoules (360ml), UDI:00850012123002 |
| Product code | MRC |
| Recalling firm | Contamac Solutions, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 7, 2023 |
| 510(k) numbers | K181566 |
| FEI number | 3016114779 |
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