Device recall
Z-1381-04: Minerva Patient Lift, model ML-20; this lift has a passive lifting unit…
FDA device recall · Class I · Medibo N.V. Heikant 5 Hanmont, Achel Belgium
Key facts
| Recall number (Z-number) | Z-1381-04 |
|---|---|
| Recall event | 29662 |
| Product | Minerva Patient Lift, model ML-20; this lift has a passive lifting unit; 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. Heikant 5 Hanmont, Achel Belgium |
| 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