Device recall
Z-0768-05: Circuit-Unilimb, Adult, 1M (40''), Disposable, Clean Non-sterile, Adult…
FDA device recall · Class II · MMS Sales Corp
Key facts
| Recall number (Z-number) | Z-0768-05 |
|---|---|
| Recall event | 31451 |
| Product | Circuit-Unilimb, Adult, 1M (40''), Disposable, Clean Non-sterile, Adult Anesthesia Circuit, Part Numbers DYNJAAF4000, DYNJAAF6225, and DYNJAAF6261. Manufactured for Medline Industries, Inc., Mundelein, IL 60060, 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