UNO 102 EM/EE/ES Patient Lift
This recall has been terminated (originally issued June 8, 2005).
- Company
- Liko, Inc.
- Recall Initiated
- September 24, 2004
- Posted
- June 8, 2005
- Terminated
- June 20, 2007
- Recall Number
- Z-0875-05
- Quantity
- 21 units
- Firm Location
- Franklin, MA
- Official Source
- View on FDA website ↗
Reason for Recall
Incorrect length support screws may cause patient lift failure
Distribution
Canada
Lot / Code Info
Serial Numbers: Range 33590-42291
Root Cause
Other
Action Taken
Liko notified Peridot Group by letter dated 9/29/04 of the recall. All Canadian distributors, including Peridot, will contact and inspect and replace bolts at user sites.
More recalls by Liko, Inc.
UNO 102 Patient Lift
Dec 13, 2005