Device recall
Z-0802-03: Non-Sterile Suture Needles, Reverse Cutting, 1/2 Circle, Stainless Steel; 12…
FDA device recall · Class II · Hu-Friedy Mfg Co, Inc.
Key facts
| Recall number (Z-number) | Z-0802-03 |
|---|---|
| Recall event | 25958 |
| Product | Non-Sterile Suture Needles, Reverse Cutting, 1/2 Circle, Stainless Steel; 12 suture needles per glass vial; partcode: SN4; Hu-Friedy Mfg. Co., Inc., 3232 N. Rockwell St., Chicago, IL 60618 |
| Product code | GAB-- |
| Recalling firm | Hu-Friedy Mfg Co, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 24, 2004 |
| FEI number | 1416605 |
At a glance
- None 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