Z-1466-2013 Class II Terminated
FDA device recall Z-1466-2013 was initiated by Hill-Rom, Inc. on Apr 15, 2013 and is designated Class II. Reason for recall: Complaints have been reported for brakes disengaging when the bed is subjected to a hard jolt or force to the frame. The recall status is terminated (terminated Feb 7, 2017). Affected quantity: 8,737 devices.
Recall Details
- Product Type
- Devices
- Report Date
- Jun 12, 2013
- Initiation Date
- Apr 15, 2013
- Termination Date
- Feb 7, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 8,737 devices
Product Description
Reason for Recall
Distribution Pattern
Worldwide distribution: US (Nationwide) and countries of: Argentina , Bahamas, Bahrain, Bolivia, Brazil, Canada, Chile, China, Colombia, Costa Rica, Ecuador, Egypt, Ethiopia, France, Ghana, Guam, Hong Kong, India, Indonesia, Japan, Jordan, Kuwait, Lebanon, Libya, Malaysia, Mexico, N. Mariana Islands, Pakistan, panama, Paraguay, Puerto Rico, Qatar, Saudi Arabia, Singapore, South Africa, South Korea, Taiwan, Thailand, United Arab Emirates, United States, US Virgin Islands, Venezuela and Vietnam.
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-1466-2013
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026