Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Handset component of the Handicare USA's Minivator Bath Bliss Reclining Recalled by Handicare Accessibility Due to Firm became aware that two handsets in the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Handicare Accessibility directly.
Affected Products
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
Why Was This Recalled?
Firm became aware that two handsets in the affected batches became inoperable while the user was in the tub.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Handicare Accessibility
Handicare Accessibility has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report