Device recall
Z-1519-2017: Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway, Catalog No. 123130…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-1519-2017 |
|---|---|
| Recall event | 76263 |
| Product | Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway, Catalog No. 123130 and 123132 Product Usage: To provide a patent airway for a patient with a blockage or potential blockage of the nasal cavity or nasopharynx. |
| Product code | BTQ |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 10, 2025 |
| FEI number | 3005747797 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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