Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Class 2 Device Recall Liko

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
  Class 2 Device Recall Liko see related information
Date Initiated by Firm November 14, 2005
Date Posted December 13, 2005
Recall Status1 Terminated 3 on February 20, 2008
Recall Number Z-0277-06
Recall Event ID 34059
Product Classification Lift, Patient, Non-Ac-Powered - Product Code FSA
Product UNO 102 Patient Lift
Code Information Serial Numbers: 33590-42291
Recalling Firm/
Manufacturer		 Liko, Inc.
842 Upper Union Street, Suite 4
Franklin MA 02038
For Additional Information Contact Anne Jordan
508-545-6671
Manufacturer Reason
for Recall		 Incorrect length leg pin bolts may cause patient lift failures
FDA Determined
Cause 2		 Other
Action 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.
Quantity in Commerce 663 units
Distribution Nationwide
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
-
-