CLASS II Device recall · Reported 18 Apr 2018 · FDA Enforcement Report
Progressa Bed - AC-powered adjustable hospital bed recalled by Hill-Rom
Hill-Rom is recalling Progressa Bed - AC-powered adjustable hospital bed, distributed nationwide in the US. The recall was initiated on 12 Jan 2018 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1319-2018
- FDA event ID
- 79516
- Recalling firm
- Hill-Rom, Batesville, IN
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 12 Jan 2018
- FDA classified
- 9 Apr 2018
- Reported
- 18 Apr 2018
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Device Malfunction
- Device type
- Wheelchairs, Beds & Lifts
Timeline
| 12 Jan 2018 | Recall initiated by company | |
| 9 Apr 2018 | Classified by FDA | +87 days |
| 18 Apr 2018 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
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.
Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.
Product as listed by the FDA
Progressa Bed - AC-powered adjustable hospital bed
Where it was distributed
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.
Questions about this recall
Why was it recalled?
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.
Which lots are affected?
S159AW9192 through S305AW2321 Beds manufactured from June 8, 2017 to November 1, 2017
Where was it sold?
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.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Hill-Rom
All 37| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Traverse Rail Carrier E-System recalled by Hill-Rom | Hill-Rom | Other | Nationwide |
| Device | CLASS II | Liko Mobile Lifts: Primarily intended for use recalled by Hill-Rom | Hill-Rom | Other | Nationwide |
| Device | CLASS II | Liko Mobile Lifts: Primarily intended for use recalled by Hill-Rom | Hill-Rom | Other | Nationwide |
| Device | CLASS II | These are communication systems, labeled as recalled by Hill-Rom | Hill-Rom | Device Malfunction | Nationwide |
| Device | CLASS II | OctoStretch with Stretch Leveller recalled by Hill-Rom | Hill-Rom | Other | Nationwide |
Other Wheelchairs, Beds & Lifts recalls
All 175| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Power F2 Powered Fastening System, Power F2 recalled by Ferno-Washington | Ferno-Washington | Potency & Assay | Nationwide |
| Device | CLASS II | Rollator, Bariatric, Basic Steel, Burgundy recalled | Medline Industries | Foreign Material | Nationwide |
| Device | CLASS II | Rollator, Bariatric, Basic Steel, Blue recalled by Medline Industries | Medline Industries | Foreign Material | Nationwide |
| Device | CLASS II | Quantum Rehab Quantum 4Front 2HD recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum Rehab Q6 Edge 2.0 (ilevel) recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |