Class II — Handicare Accessibility
| Recalling firm | Handicare Accessibility |
|---|---|
| Registered facility | Savaria Lifts (UK) Ltd. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Firm became aware that two handsets in the affected batches became inoperable while the user was in the tub. |
| 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 patient lift consisting of a motorized actuator, powered mechanical seating device, temporarily secured in a bath, and used to lift and lower a patient in the vertical or reclining position while bathing. |
| Quantity | 3301 handsets |
| Distribution | Worldwide distribution: USA (Nationwide) and country of: Canada. |
| Initiated | 2012-11-29 |
| Classified | 2013-11-06 |
| Terminated | 2014-12-08 |
| Recall number | Z-0171-2014 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Handicare Accessibility (Z-0171-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/63859/
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