Drug recall
Laerdal Compact Suction Unit (LCSU 4), Catalog Numbers 880051, 880061, 881151, 880052, 880062, 881152…
FDA recall event 86702 · Class II · Laerdal Medical (Suzhou) Co., Ltd.
Key facts
| Event ID | 86702 |
|---|---|
| Recall numbers | Z-0868-2021 |
| Recalling firm | Laerdal Medical (Suzhou) Co., Ltd. |
| Product type | Devices |
| Products | 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… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Component failures may cause the unit to lose all suction. Users will need to obtain alternate suction devices or methods, leading to a delay in treatment and, in worst case scenario, potential… |
| Initiation date | Dec 18, 2020 |
| Report date | Jan 27, 2021 |
| Termination date | Dec 11, 2023 |
| City | Suzhou |
| Country | China |
| FEI number | 3004993040 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: