Device recall
Z-0260-05: XPRT Therapy Mattress Systems: Model # 2950-000-000 with Dartex urethane-coated…
FDA device recall · Class II · Gaymar Industries Inc
Key facts
| Recall number (Z-number) | Z-0260-05 |
|---|---|
| Recall event | 30065 |
| Product | XPRT Therapy Mattress Systems: Model # 2950-000-000 with Dartex urethane-coated nylon cover (deluxe cover); and Model # 2950-000-001 with nylon cover without coating (standard cover). Responsible firm on the label: Manufactured for STRYKER MEDICAL, 6300 South Sprinkle Road, Kalamazoo, MI USA… |
| Product code | IKZ |
| Recalling firm | Gaymar Industries Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 8, 2006 |
| FEI number | 1313850 |
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