Device recall
Z-0712-05: MEDPOR Surgical Implant * POREX Surgical Products Group * Sterile/EO * Implant…
FDA device recall · Class III · Porex Surgical, Inc.
Key facts
| Recall number (Z-number) | Z-0712-05 |
|---|---|
| Recall event | 31604 |
| Product | MEDPOR Surgical Implant * POREX Surgical Products Group * Sterile/EO * Implant, Non-Pyrogenic, For Single Use Only, CAT #6317 DIM 20mm Diameter * Lot xxxxxx * QTY: 1 * Porex Surgical Inc., 15 Dart Road, Newnan, GA 30265 USA |
| Product code | HPZ |
| Recalling firm | Porex Surgical, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 17, 2005 |
| 510(k) numbers | K863943 |
| FEI number | 1000131961 |
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