Device recall
Z-0770-05: Medline Custom Anesthesia Super Circuit Adult 60 Unilimb Kit (non-sterile)…
FDA device recall · Class II · Medline Industries, Inc.
Key facts
| Recall number (Z-number) | Z-0770-05 |
|---|---|
| Recall event | 31528 |
| Product | Medline Custom Anesthesia Super Circuit Adult 60 Unilimb Kit (non-sterile), reorder number DYNJAAF6267; the kit contains the Nexus Adult Unilimb Circuit - 60'', part 60010-1B, along with a 3 liter latex breathing bag, anesthesia tubing clip, suction catheter, adult anesthesia mask, suction canister… |
| 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