Device recall
Z-1105-2012: Premier LifeCare Recliner 5400. Brochure is labeled in part: "***Premier…
FDA device recall · Class II · Winco Mfg., LLC
Key facts
| Recall number (Z-number) | Z-1105-2012 |
|---|---|
| Recall event | 61049 |
| Product | Premier LifeCare Recliner 5400. Brochure is labeled in part: "***Premier LifeCare Recliner 5400***Winco***ISO 9001 2008 Certified***Key Features***Urethane armrests***Fully upholstered***Multiple side-table Options***3-position lockbar*** "No pinch" safety zone***1.800.237.3377***5516 SW 1st… |
| Product code | INM |
| Recalling firm | Winco Mfg., LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 4, 2012 |
| FEI number | 1027229 |
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