Device recall
Z-1927-2012: AirLife MiniSpacer MDI Dispenser Adapter. Dual-Spray MiniSpacer Metered Dose…
FDA device recall · Class II · Thayer Medical Corporation
Key facts
| Recall number (Z-number) | Z-1927-2012 |
|---|---|
| Recall event | 62283 |
| Product | AirLife MiniSpacer MDI Dispenser Adapter. Dual-Spray MiniSpacer Metered Dose Inhaler (MDI) Dispenser/Adapter with 15 mm connections. The 15 mm Dual Spray MiniSpacer is a Metered Dose Inhaler (MDI) Dispenser. It is a non-sterile, single-use item, intended to dispense aerosolized medication into a… |
| Product code | CAF |
| Recalling firm | Thayer Medical Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 15, 2013 |
| 510(k) numbers | K955805 |
| FEI number | 2026894 |
At a glance
- 1–9 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