Z-0872-2013 Class II Terminated
FDA device recall Z-0872-2013 was initiated by Hill-Rom, Inc. on Oct 31, 2012 and is designated Class II. Reason for recall: Liko/Hill-Rom to date has received two reports from facilities alleging that the overhead rail system has failed to the extent that the overhead rails have fallen down while in use in high humidity… The recall status is terminated (terminated Mar 9, 2016). Affected quantity: 3816 in total.
Recall Details
- Product Type
- Devices
- Report Date
- Feb 27, 2013
- Initiation Date
- Oct 31, 2012
- Termination Date
- Mar 9, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 3816 in total
Product Description
Liko Overhead Rail System, Ceiling Mounted Rail Systems for all Liko Stationary Lifts including Likorall, Multirall and Masterlift Systems Product Usage - The Overhead Rail System allows overhead lifts to be mounted to the ceiling allowing versatility for use in lifting situations. It can be used with different Liko ceiling lifts.
Reason for Recall
Liko/Hill-Rom to date has received two reports from facilities alleging that the overhead rail system has failed to the extent that the overhead rails have fallen down while in use in high humidity (swimming pool) areas. Analysis of the incidents suggest that the components (hardware) used to secure the rail to the ceiling had corroded and may be unsuitable for environments with an atmosphere con
Distribution Pattern
Worldwide Distribution: USA (nationwide) including states of: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, and WY; and CANADA LOCATIONS: AB, BC, MB, NB, NS, ON, and SK.
Code Information
The Liko Overhead Rail System components are not serialized and have been distributed since the early 1980's to the present.
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0872-2013
- openFDA file date
- Oct 26, 2026
- Loaded by RegDataLab
- Oct 27, 2026