Product Wiki · Recalls · U.S. FDA — Device Enforcement

Progressa Bed - AC-powered adjustable hospital bed — recall Z-1319-2018

U.S. FDA — Device Enforcement · United States · 2018-01-12 · Class II

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1319-2018
Date of alert
2018-01-12
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Hill-Rom, Inc.
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

Related

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.