Device recall
Z-2294-2019: TiLite X-Short anti-tip tubes, models TRA, AERO T, ZRA, AERO Z, 2GX, AERO X…
FDA device recall · Class II · TiSport, Llc
Key facts
| Recall number (Z-number) | Z-2294-2019 |
|---|---|
| Recall event | 83360 |
| Product | TiLite X-Short anti-tip tubes, models TRA, AERO T, ZRA, AERO Z, 2GX, AERO X, Twist, and AERO R, a component of the TiLite wheelchair (anti-tip extension for manual wheelchairs). Product Usage: The affected component is part of a manual wheelchair to provide mobility to physically impaired… |
| Product code | IOR |
| Recalling firm | TiSport, Llc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 29, 2022 |
| 510(k) numbers | K023606, K072311, K990358 |
| FEI number | 3002653226 |
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