Hill-Rom, Inc.: Medical Device Recall in 2018 - (Recall #: Z-1319-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Progressa Bed - AC-powered adjustable hospital bed

Product Classification:

Class II

Date Initiated: January 12, 2018

Date Posted: April 18, 2018

Recall Number: Z-1319-2018

Event ID: 79516

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.

Status: Terminated

Product Quantity: 2117

Code Information:

S159AW9192 through S305AW2321 Beds manufactured from June 8, 2017 to November 1, 2017

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.

Voluntary or Mandated:

Voluntary: Firm initiated