Device recall
Z-0868-2021: Laerdal Compact Suction Unit (LCSU 4), Catalog Numbers 880051, 880061, 881151…
FDA device recall · Class II · Laerdal Medical (Suzhou) Co., Ltd.
Key facts
| Recall number (Z-number) | Z-0868-2021 |
|---|---|
| Recall event | 86702 |
| Product | Laerdal Compact Suction Unit (LCSU 4), Catalog Numbers 880051, 880061, 881151, 880052, 880062, 881152 - Product Usage: It is intended for intermittent operation to remove secretions, blood or vomit from a patient s airway to allow ventilation. |
| Product code | JCX |
| Recalling firm | Laerdal Medical (Suzhou) Co., Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 11, 2023 |
| 510(k) numbers | K120065 |
| FEI number | 3004993040 |
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