Aidacare Aspire Mobile Patient Lifter - Powered
- Recalling firm
- Compliance Management Solutions NZ
- Product
- Aidacare Aspire Mobile Patient Lifter - Powered. [Device]. Model: Aidacare Aspire Aura and Nova Lifters. Affected: Item Numbers: LSS390615 & LSS390652 - (serial numbers prior to XXX-PO01260162-0000)
- Reason
- The manufacturer has identified that the bolts securing the leg-spread actuators to the lifter frame can gradually loosen over time with regular use. If not addressed, this may lead to bolt detachment. As a result, one or both legs may become decoupled from the actuators and move freely when push or pull forces are applied to manoeuvre the lifter., If this occurs, users may experience difficulties when moving the lifter - whether or not a patient is suspended. The lifter may veer or pull noticeably toward the affected leg when force is applied, impacting safe and controlled operation.
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-03-10
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/cbcdd849-69ce-495c-9826-50caecb7a804