Recall Z-0171-2014— Handicare Accessibility
Class II · Terminated
Class II FDA medical device recall by Handicare Accessibility, initiated 2012-11-29, terminated 2014-12-08. FDA's recall record names no specific 510(k) clearance for this event. 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.. Reason: Firm became aware that two handsets in the affected batches became inoperable while the user was in the tub..
- Recalling firm
- Handicare Accessibility
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2012-11-29
- Terminated
- 2014-12-08
- Firm location
- Allentown, PA, United States
Product description
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.
Reason for recall
Firm became aware that two handsets in the affected batches became inoperable while the user was in the tub.
Data sourced from openFDA. This site is unofficial and independent of the FDA.