Device recall
Z-0771-05: Medline Custom Anesthesia Set Up Kit - Latex Free (non-sterile), reorder number…
FDA device recall · Class II · Medline Industries, Inc.
Key facts
| Recall number (Z-number) | Z-0771-05 |
|---|---|
| Recall event | 31528 |
| Product | Medline Custom Anesthesia Set Up Kit - Latex Free (non-sterile), reorder number DYNJAA0078C; the kit contains the Nexus Adult Unilimb Circuit - 40'', part C4N000D001, along with a 3 liter latex free breathing bag, suction catheter, adult medium anesthesia mask, suction tubing, humid vent hme filter… |
| Product code | LRO |
| Recalling firm | Medline Industries, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 17, 2005 |
| FEI number | 3000717925 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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