notyard
04-14-2009, 02:22 PM
FDA class II recall:
PRODUCT
Ergolift 400 Lbs. Floor Lift, model/part numbers ERGOLIFT and ERGOLIFT-2. The equipment is intended to be used in hospitals, nursing homes, or other health care facilities by trained caregivers for the transfer of patients. Recall # Z-0933-2009
CODE
Serial numbers: ERLI-0001 through ERLI-1717, manufactured between 1995 and 1999
RECALLING FIRM/MANUFACTURER
Recalling Firm: Arjo, Inc., Roselle , IL , by Field Safety Notice dated December 8, 2008 and letter dated December 22, 2008.
Manufacturer: B.H.M. Medical, Inc., Magog , Canada . Firm initiated recall is ongoing.
REASON
Report of structural failure of the mast during use.
VOLUME OF PRODUCT IN COMMERCE
220 lifts
DISTRIBUTION
Nationwide
PRODUCT
Ergolift 400 Lbs. Floor Lift, model/part numbers ERGOLIFT and ERGOLIFT-2. The equipment is intended to be used in hospitals, nursing homes, or other health care facilities by trained caregivers for the transfer of patients. Recall # Z-0933-2009
CODE
Serial numbers: ERLI-0001 through ERLI-1717, manufactured between 1995 and 1999
RECALLING FIRM/MANUFACTURER
Recalling Firm: Arjo, Inc., Roselle , IL , by Field Safety Notice dated December 8, 2008 and letter dated December 22, 2008.
Manufacturer: B.H.M. Medical, Inc., Magog , Canada . Firm initiated recall is ongoing.
REASON
Report of structural failure of the mast during use.
VOLUME OF PRODUCT IN COMMERCE
220 lifts
DISTRIBUTION
Nationwide