Liko, Inc. UNO 102 EM/EE/ES Patient Lift Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
UNO 102 EM/EE/ES Patient Lift
Brand
Liko, Inc.
Lot Codes / Batch Numbers
Serial Numbers: Range 33590-42291
Products Sold
Serial Numbers: Range 33590-42291
Liko, Inc. is recalling UNO 102 EM/EE/ES Patient Lift due to Incorrect length support screws may cause patient lift failure. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Incorrect length support screws may cause patient lift failure
Recommended Action
Per FDA guidance
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.
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