Z-1319-2018 Class II Terminated
FDA device recall Z-1319-2018 was initiated by Hill-Rom, Inc. on January 12, 2018 and is designated Class II. Reason for recall: A component used within the braking system may break resulting in one or more brake pedals on the bed staying in brake or not being engaged which could result in unwanted bed movement and possible pat… The recall status is terminated (terminated June 26, 2020). Affected quantity: 2117.
Recall Details
- Product Type
- Devices
- Report Date
- April 18, 2018
- Initiation Date
- January 12, 2018
- Termination Date
- June 26, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2117
Product Description
Progressa Bed - AC-powered adjustable hospital bed
Reason for Recall
A component used within the braking system may break resulting in one or more brake pedals on the bed staying in brake or not being engaged which could result in unwanted bed movement and possible patient or user injury.
Distribution Pattern
Worldwide distribution. US nationwide, Canada, Chile, Colombia, Costa Rica, France, Hong Kong, Israel, Jamaica, Japan, Jordan, Malaysia, Mexico, Oman, Panama, Russian Federation, Saudi Arabia, Singapore, Spain, Taiwan, UAE, and UK.
Code Information
S159AW9192 through S305AW2321 Beds manufactured from June 8, 2017 to November 1, 2017