Device recall
Z-0519-04: LAERDAL Silicone Resuscitator (LSR), Preterm Size, containing an…
FDA device recall · Class II · Laerdal Medical Corporation
Key facts
| Recall number (Z-number) | Z-0519-04 |
|---|---|
| Recall event | 28029 |
| Product | LAERDAL Silicone Resuscitator (LSR), Preterm Size, containing an Intake/Reservoir Valve. Sold as Part Nos: 850050-Preterm Basic w/o Mask in Carton; 850051-Preterm Complete in Carton; 850053-Preterm Complete in Compact Case; 850055-Preterm Complete in Display Case; 855500-Preterm Update Kit… |
| Product code | BTM |
| Recalling firm | Laerdal Medical Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 16, 2005 |
| 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