Device recall
Z-1873-2017: Laerdal Compact Suction Unit 4 under the following labels: 1) 300 ml (3.3 lbs)…
FDA device recall · Class II · Laerdal Medical Corporation
Key facts
| Recall number (Z-number) | Z-1873-2017 |
|---|---|
| Recall event | 76744 |
| Product | Laerdal Compact Suction Unit 4 under the following labels: 1) 300 ml (3.3 lbs) canister version - CATALOG #(s): 88006101 - LCSU 4, 300 ml Complete unit (US), 88006103 - LCSU 4, 300 ml Complete unit (UK), 88006140 - LCSU 4, 300 ml Complete unit (EUR), 881151 - Replacement unit, 88006201 - LCSU 4, 300… |
| Product code | JCX |
| Recalling firm | Laerdal Medical Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 25, 2018 |
| FEI number | 2425852 |
At a glance
- None 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