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Use caution Medical device recall · FDA · Published January 12, 2018

Hill-Rom Progressa Bed Recall: Brake Failure Risk

Hill-Rom recalls AC-powered adjustable hospital beds from June 2017 due to brake system failure risk. Affected models S159AW9192 to S305AW2321 may cause bed movement and patient injury if brakes malfunction.

🇺🇸 FDA recall #Z-1319-2018Medical deviceHill-Rom ›
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Recalling firmHill-Rom, Inc.1069 State Road 46 E · Batesville, IN 47006-7520
✎ GovInfoNow plain-language explainer

Hill-Rom is recalling AC-powered hospital beds made between June 2017 and November 2017 because a brake component could break, causing the bed to move unexpectedly and potentially injuring patients or users. Read more at govinfonow.com/recall/72142-hill-rom-progressa-bed-recall-brake-failure-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/72142-hill-rom-progressa-bed-recall-brake-failure-risk · Updated August 31, 2026 · FDA enforcement record: FDA #Z-1319-2018

Cite this page

“Hill-Rom Progressa Bed Recall: Brake Failure Risk.” GovInfoNow, updated August 31, 2026. https://govinfonow.com/recall/72142-hill-rom-progressa-bed-recall-brake-failure-risk. Based on FDA recall #Z-1319-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1319-2018%22&limit=1).

The FDA announced on Jan. 12, 2018, that Hill-Rom, Inc. is recalling Progressa AC-powered adjustable hospital beds due to a braking system component failure. This defect could cause unwanted bed movement and potential injury to patients or users.

How to tell if you have it

  • Brand: Hill-Rom
  • Product: Progressa Bed - AC-powered adjustable hospital bed
  • Model numbers: S159AW9192 through S305AW2321
  • Manufacture dates: June 8, 2017 to November 1, 2017

The hazard

A component within the braking system may break, causing one or more brake pedals to stay in brake or not engage. This could result in unwanted bed movement and possible patient or user injury.

Context

GovInfoNow's records show Hill-Rom, Inc. has had 9 other recalls since Feb. 14, 2020. Recent Hill-Rom recalls include Traverse Rail Carriers (Jan. 14, 2022), Liko M220 Lifts (Dec. 23, 2021), and NaviCare/Voalte Nurse Call Systems (Oct. 14, 2021). Other recent recalls of similar products include WHILL Wheelchairs (Dec. 29, 2025), Medline Bariatric Rollator (Aug. 14, 2026), and Baxter Healthcare PRO+ 40" MRS SURFACE Mattress (Aug. 18, 2026).

How to tell if you have this one

Check for model numbers starting with S159AW9192 through S305AW2321. These beds were manufactured between June 8, 2017 and November 1, 2017.

  • Brand
    Hill-Rom
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Model Number

    Look for model numbers starting with S159AW9192 through S305AW2321 on the bed's label.

  2. Contact Hill-Rom

    Reach out to Hill-Rom directly for assistance with the recall process.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “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.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 2.5 years after the firm started it.

1. Firm started the recall: Jan 12, 201812. FDA classified it Class II: Apr 9, 201823. Published in FDA’s Enforcement Report: Apr 18, 201834. FDA terminated the recall: Jun 26, 2020420182020
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-1319-2018 (January 12, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1319-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on August 31, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA