Device recall
Z-0576-03: Convertors Three Quarter Sheet (Drape Sheet), catalog #29350; Allegiance…
FDA device recall · Class II · Allegiance Healthcare Corp.
Key facts
| Recall number (Z-number) | Z-0576-03 |
|---|---|
| Recall event | 25475 |
| Product | Convertors Three Quarter Sheet (Drape Sheet), catalog #29350; Allegiance Healthcare Corporation, McGaw Park, IL 60085 USA; individually packaged drapes, 20 packages per case |
| Product code | KKX-- |
| Recalling firm | Allegiance Healthcare Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 3, 2003 |
| 510(k) numbers | K002419 |
| FEI number | 3001236905 |
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