Device recall
Z-1868-2021: Adult-Pediatric Electrostatic Filter HME, Item Code 352/5877Z - Product Usage…
FDA device recall · Class II · Covidien, LP
Key facts
| Recall number (Z-number) | Z-1868-2021 |
|---|---|
| Recall event | 87925 |
| Product | Adult-Pediatric Electrostatic Filter HME, Item Code 352/5877Z - Product Usage: indicated for single use on anesthetized patients and respiratory care patients who require a breathing circuit with ISO standard 15mm or 22 mm connectors. |
| Product code | CAH |
| Recalling firm | Covidien, LP |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K941535 |
| FEI number | 1219930 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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