Device recall
Z-0518-04: LAERDAL Silicone Resuscitator (LSR), Pediatric Size, containing an…
FDA device recall · Class II · Laerdal Medical Corporation
Key facts
| Recall number (Z-number) | Z-0518-04 |
|---|---|
| Recall event | 28029 |
| Product | LAERDAL Silicone Resuscitator (LSR), Pediatric Size, containing an Intake/Reservoir Valve. Sold as Part Nos: 860050-Pediatric Basic w/o Mask in Carton; 860051-Pediatric Complete in Carton; 860052-Standard Child w/Child Mask 3-4 in Carton; 860053-Pediatric Complete in Compact Case; 860055-Pediatric… |
| 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