Device recall
Z-1341-2026: Laerdal Compact Suction Unit 4 RTCA version (LCSU 4 RTCA) 1) LCSU 4, 800 ml…
FDA device recall · Class II · Laerdal Medical Corporation
Key facts
| Recall number (Z-number) | Z-1341-2026 |
|---|---|
| Recall event | 98039 |
| Product | Laerdal Compact Suction Unit 4 RTCA version (LCSU 4 RTCA) 1) LCSU 4, 800 ml, RTCA; Catalog Number: 880052; 2) LCSU 4, 300 ml, RTCA; Catalog Number: 880062; 3) LCSU 4, RTCA; Catalog Number: 881152; |
| Product code | JCX |
| Recalling firm | Laerdal Medical Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K120065 |
| FEI number | 2425852 |
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