Device recall
Z-0517-04: LAERDAL Silicone Resuscitator (LSR), Adult size, containing Intake/Reservoir…
FDA device recall · Class II · Laerdal Medical Corporation
Key facts
| Recall number (Z-number) | Z-0517-04 |
|---|---|
| Recall event | 28029 |
| Product | LAERDAL Silicone Resuscitator (LSR), Adult size, containing Intake/Reservoir Valve. Sold as Part Nos: 870050-Adult Basic w/o Mask in Carton; 870051-Adult Complete in Carton; 870052-Adult Standard with Adult Mask 4-5+ in Carton; 870053-Adult Complete in Compact Case; 870055-Adult Complete in Display… |
| 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