Device recall
Z-0171-2014: Handset component of the Handicare USA's Minivator Bath Bliss Reclining Bath…
FDA device recall · Class II · Handicare Accessibility
Key facts
| Recall number (Z-number) | Z-0171-2014 |
|---|---|
| Recall event | 63859 |
| Product | Handset component of the Handicare USA's Minivator Bath Bliss Reclining Bath Lifts (Bath Bliss), Part Number BP300-100/BP300-400RSUS (handset) - Model Numbers BBR0311USAB (blue) and BBR0311USSS (silver) Handset component devices operate the Minivator Bath Bliss Reclining Bath Lift, a non-AC-powered… |
| Product code | FSA |
| Recalling firm | Handicare Accessibility |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 8, 2014 |
| FEI number | 3007802293 |
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