Device recall
Z-1053-03: LMA- Unique Laryngeal Mask Airway Size 4, Catalog No. 12140, Lot FH041202 Size…
FDA device recall · Class II · LMA North America Inc
Key facts
| Recall number (Z-number) | Z-1053-03 |
|---|---|
| Recall event | 26577 |
| Product | LMA- Unique Laryngeal Mask Airway Size 4, Catalog No. 12140, Lot FH041202 Size 4, Catalog No. 12150, Lot FJ021202 |
| Product code | CAE |
| Recalling firm | LMA North America Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 3, 2003 |
| FEI number | 3001338204 |
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