Device recall
Z-0015-2012: Custom anesthesia kits labeled as follows: (1) DeRoyal (R) Adult Exp Anesthesia…
FDA device recall · Class II · Deroyal Industries, Inc. Lafollette
Key facts
| Recall number (Z-number) | Z-0015-2012 |
|---|---|
| Recall event | 59854 |
| Product | Custom anesthesia kits labeled as follows: (1) DeRoyal (R) Adult Exp Anesthesia Circuit, REF 86-001737, Rx Only, NON-STERILE, Manufactured by: DeRoyal Industries, Inc. 200 DeBusk Lane, Powell, TN 37849, USA; Lot Number 25660996 (2) DeRoyal (R) Adult Anesthesia Circuit, REF 86-001781, Rx Only… |
| Product code | OGD |
| Recalling firm | Deroyal Industries, Inc. Lafollette |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 30, 2013 |
| FEI number | 3005011024 |
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