Device recall
Z-0323-2010: 24CM ALTA LR STANDARD KIT Model: AL19NH24 ALTA CATHETER WITH NO SIDE HOLES 15.5…
FDA device recall · Class II · Spire Biomedical, Inc.
Key facts
| Recall number (Z-number) | Z-0323-2010 |
|---|---|
| Recall event | 53605 |
| Product | 24CM ALTA LR STANDARD KIT Model: AL19NH24 ALTA CATHETER WITH NO SIDE HOLES 15.5 Fr polyurethane twin lumen fixed tip hemodialysis catheter, cuff, and no side holes for chronic hemodialysis and apheresis. Kit contains catheter, 18 gauge introducer needle,12cc syringe, J/straight 0.038 inch x 100 cm… |
| Product code | MSD |
| Recalling firm | Spire Biomedical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 9, 2010 |
| 510(k) numbers | K032061, K040509, K042858, K060155, K063431, K063441 |
| FEI number | 1000159376 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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