Aidacare Aspire Mobile Patient Lifter - Powered

Aidacare Aspire Mobile Patient Lifter - Powered Recall Summary Aidacare is updating the instructions for use for the Aspire Mobile Patient Lifter - Powered. This Class I recall affects units distributed to hospitals, pharmacies, and laboratories in New Zealand. The company has not specified what changes are being made to the instructions.

Recalling firm

Compliance Management Solutions NZ

Product

Aidacare Aspire Mobile Patient Lifter - Powered. [Device]. Model: Aidacare Aspire A205 Aluminium Patient Lifter. Affected: Item Numbers: LSS390610

Reason

The manufacturer has identified that improper attachment of slings to the lifter's sling bar can cause patients to fall, sustaining severe injuries or death. Aidacare has enhanced the instructions for use (IFU) to strengthen existing instructions around correct and incorrect sling attachment methods and pre-use checks.

Classification

Class I

Category

medical device recall

Country

New Zealand

Agency

MEDSAFE

Recall date

2026-06-08

Status

Ongoing

Distribution

New Zealand - Hospital/Pharmacy/Laboratory

Official recall notice from MEDSAFE

Recall details on Nibble Recalls: https://trynibble.app/recalls/a945eed6-324c-486e-872c-a5667b4cef78