Device recall
Z-0464-2014: Centurion Sterile # 84 Rubber Bands Reorder EB84, Caution: This product contains…
FDA device recall · Class II · Centurion Medical Products Corporation
Key facts
| Recall number (Z-number) | Z-0464-2014 |
|---|---|
| Recall event | 66830 |
| Product | Centurion Sterile # 84 Rubber Bands Reorder EB84, Caution: This product contains natural rubber latex which may cause allergic reactions. LATEX FREE , CAUTION: FEDERAL lAW (USA) RESTRICTS THIS DEVICE TO SALE BY OR ON THE ORDER OF A PHYSICIAN Single Use Only bands items together and podiatry office… |
| Product code | LDQ |
| Recalling firm | Centurion Medical Products Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 29, 2014 |
| FEI number | 1824619 |
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