Device recall
Z-2254-2024: BAUSCH+LOMB, I-PACK Injection Kit with Wire Speculum, REF 18069W, for the…
FDA device recall · Class I · Synergetics Inc
Key facts
| Recall number (Z-number) | Z-2254-2024 |
|---|---|
| Recall event | 94793 |
| Product | BAUSCH+LOMB, I-PACK Injection Kit with Wire Speculum, REF 18069W, for the administration of intravitreal injection (eye) |
| Product code | KDD |
| Recalling firm | Synergetics Inc |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 1000119053 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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