LMA North America Inc
LMA North America Inc appears in FDA public data with 1 recall, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2022-2012, Class II) was initiated on May 23, 2012.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-2022-2012 | Class II | LMA Esophageal Intubation Detector (EID), Catalog Number EID100 The device is used to assist veri | May 23, 2012 |