Atlas FDA

Sunrise Hoyer Advance Patient lifts

FDA device recall Z-0785-05 · posted 2005-05-03 · Terminated

Recall details

Recalling firm
Sunrise Medical, Inc.
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.
Action taken
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
Status
Terminated
Product code
FSA
Quantity affected
27 units
Distribution
Domestic distribution: WI, FL, GA, TX, OK. Foreign distribution: Canada. No military or VA facilities
Date initiated
2005-02-03
Date posted
2005-05-03
Date terminated
2005-08-08
Location
Longmont, CO

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