Medical DevicesNationwide
Liko, Inc. UNO 102 Patient Lift Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
UNO 102 Patient Lift
Brand
Liko, Inc.
Lot Codes / Batch Numbers
Serial Numbers: 33590-42291
Products Sold
Serial Numbers: 33590-42291
Liko, Inc. is recalling UNO 102 Patient Lift due to Incorrect length leg pin bolts may cause patient lift failures. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Incorrect length leg pin bolts may cause patient lift failures
Recommended Action
Per FDA guidance
Liko Inc. initiated the recall to Distributors of the Recall on 11/14/05 via UPS. Direct customers will be notified by letter on /about 12/1/05.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026