Device recall
Z-1280-03: Phaco Needles, catalog #DP8115, with 15 degree needle taper, labeld in…
FDA device recall · Class II · Bausch & Lomb Incorporated
Key facts
| Recall number (Z-number) | Z-1280-03 |
|---|---|
| Recall event | 27058 |
| Product | Phaco Needles, catalog #DP8115, with 15 degree needle taper, labeld in part***Non-sterile, Manufactured for Bausch and Lomb, Inc. Rochester, NY 14609***, packaged 6 needles/box. |
| Product code | HQC |
| Recalling firm | Bausch & Lomb Incorporated |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 15, 2003 |
| 510(k) numbers | K952259 |
| FEI number | 1000305478 |
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