Z-1473-2013 Class II Terminated
FDA device recall Z-1473-2013 was initiated by Hill-Rom, Inc. on Apr 30, 2013 and is designated Class II. Reason for recall: Retrospective review found 4 sling bars that may present a potential for impalement if a patient, caregiver or bystander were to fall onto the hooks based on a simulated test method. In effort to… The recall status is terminated (terminated Nov 28, 2014). Affected quantity: 3556.
Recall Details
- Product Type
- Devices
- Report Date
- Jun 12, 2013
- Initiation Date
- Apr 30, 2013
- Termination Date
- Nov 28, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 3556
Product Description
Reason for Recall
Distribution Pattern
Worldwide Distribution-USA (nationwide) including the states of AZ, CA, CO, FL, IL, IN, KS, LA, MA, MI, MN, MO, NC, NH, NJ, NV, OH, OK, PA, SC, TN, UT, WA, and WI, and the countries of Canada, Australia, Austria, Belgium, Switzerland, Germany Denmark, Spain, Finland, France, United Kingdom, Greece, Hong Kong, Ireland, Israel, Italy, Japan, Netherlands, Norway, New Zealand, Portugal, Sweden, and Turkey.
Code Information
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1473-2013
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026