Device recall
Z-0383-2017: FLEXI NOZZLE SHORT Product Usage: These products are used for the delivery of…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-0383-2017 |
|---|---|
| Recall event | 75554 |
| Product | FLEXI NOZZLE SHORT Product Usage: These products are used for the delivery of topical anesthesia via an atomized spray to the oral, nasal, pharyngeal or laryngeal mucosa. Teleflex Medical is recalling these products as they may produce a straight stream instead of a fully atomized plume of… |
| Product code | CCQ |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 25, 2020 |
| 510(k) numbers | K153470 |
| FEI number | 3005747797 |
At a glance
- 1–9 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