Device recall
Z-2440-2008: 500 mL InfoV.A.C. Canister (without Gel); Part #M8275071/5 (5 canister pack) and…
FDA device recall · Class II · KCI USA, Inc.
Key facts
| Recall number (Z-number) | Z-2440-2008 |
|---|---|
| Recall event | 49110 |
| Product | 500 mL InfoV.A.C. Canister (without Gel); Part #M8275071/5 (5 canister pack) and Part #M8275071/10 (10 canister pack); products are single use and labeled as STERILE; distributed by Kinetic Concepts, Inc., San Antonio, TX. |
| Product code | JCX |
| Recalling firm | KCI USA, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 13, 2009 |
| 510(k) numbers | K063740 |
| FEI number | 1625774 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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