Device recall
Z-2022-2012: LMA Esophageal Intubation Detector (EID), Catalog Number EID100 The device is…
FDA device recall · Class II · LMA North America Inc
Key facts
| Recall number (Z-number) | Z-2022-2012 |
|---|---|
| Recall event | 62337 |
| Product | LMA Esophageal Intubation Detector (EID), Catalog Number EID100 The device is used to assist verification of placement of the endotracheal tube or esophageal/tracheal double lumen tube. This device is to be used as an adjunct to assess intubation. Its purpose is not to eliminate clinical judgment |
| Product code | BTR |
| Recalling firm | LMA North America Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 26, 2012 |
| 510(k) numbers | K930741 |
| FEI number | 3001338204 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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