Device recall
Z-0764-05: Portex Adult Single Limb Anesthesia Breathing Circuit, single use, Part Numbers…
FDA device recall · Class II · MMS Sales Corp
Key facts
| Recall number (Z-number) | Z-0764-05 |
|---|---|
| Recall event | 31451 |
| Product | Portex Adult Single Limb Anesthesia Breathing Circuit, single use, Part Numbers: 386000 and 384001. Manufactured for Sims Portex, Inc., Fort Meyers, FL, Made in Mexico. |
| Product code | CAI |
| Recalling firm | MMS Sales Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 20, 2006 |
| FEI number | 3004752896 |
At a glance
- None Linked 510(k)s
- 1–9 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