Device recall
Z-1755-2024: Johnson & Johnson VISION Reusable LAMINAR High Flow Irrigation Sleeve and Test…
FDA device recall · Class II · Johnson & Johnson Surgical Vision, Inc.
Key facts
| Recall number (Z-number) | Z-1755-2024 |
|---|---|
| Recall event | 94231 |
| Product | Johnson & Johnson VISION Reusable LAMINAR High Flow Irrigation Sleeve and Test Chamber 21 Gauge REF OPOHF21L The irrigation sleeve is a device intended to direct irrigation solution across the shaft of a phacoemulsification tip, allowing the solution to enter the eye during ocular surgery. |
| Product code | HQC |
| Recalling firm | Johnson & Johnson Surgical Vision, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K121721 |
| FEI number | 3012236936 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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