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Terminated

Sunrise Hoyer Advance Patient lifts

FDA Recall Z-0785-05 · Posted 2005-05-03

Recalling FirmSunrise Medical, Inc.
Recall StatusTerminated
Product CodeFSA
Date Initiated2005-02-03
Date Terminated2005-08-08
Product Quantity27 units

Reason for Recall

The leg actuation mechanism on certain Hoyer Advance Patient Lifts may not operate properly, which could cause the lift to become unstable.

Firm Action

Telephone calls were placed to customers on 02/03/05. Urgent Medical Device Correction letters, dated 02/03/05, were also sent to customers.

Root Cause

Other

Distribution Pattern

Domestic distribution: WI, FL, GA, TX, OK. Foreign distribution: Canada. No military or VA facilities

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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