Device recall
Z-0262-2020: POM Procedural Oxygen Masks, Endoscopic, Conscious Sedation, Bronchoscopy Mask…
FDA device recall · Class II · POM Medical LLC
Key facts
| Recall number (Z-number) | Z-0262-2020 |
|---|---|
| Recall event | 83540 |
| Product | POM Procedural Oxygen Masks, Endoscopic, Conscious Sedation, Bronchoscopy Mask, as follows: (1) POM Medical, LLC, REF 1001-MM, High/Med Concentrations, Distributed by POM Medical, LLC, Moorpark, CA; (2) curaplex, REF 301-0318LT, Medium Concentration, Distributed by Sarnova HC, LLC's family of… |
| Product code | BYG |
| Recalling firm | POM Medical LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 4, 2021 |
| FEI number | 3010411911 |
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