Device recall
Z-1381-04: Minerva-Combi Patient Lift, model ML-30; this lift comes with interchangable…
FDA device recall · Class I · Medibo N.V.
Key facts
| Recall number (Z-number) | Z-1381-04 |
|---|---|
| Recall event | 29662 |
| Product | Minerva-Combi Patient Lift, model ML-30; this lift comes with interchangable passive and active lifting units; Manufactured by Medibo-Technics, Hasseltsebaan 24, 3940 Hechtel-Eksel, Belgium and distributed by MasterCare Patient Equipment, Inc., Hwy 61 West Industrial Park, Columbus, NE 68601 |
| Product code | FSA |
| Recalling firm | Medibo N.V. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Dec 13, 2004 |
| FEI number | 3004468271 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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