Use caution Medical device recall · FDA · Published June 30, 2020

Hill-Rom Progressa Bed Recall: Screw Failure Risk for Patient Injury

Hill-Rom recalls Progressa Bed model P7500 (serials V133AW9885-V142AW0261) manufactured May 2020 due to potential screw failure causing serious injury during medical use.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2737-2020Medical device Hill-Rom ›

Use caution until it’s fixed

Affected beds may have screws installed that do not meet material tensile strength requirements. Failure of this screw could result in serious patient or user injury.

Take action

Contact the company

Recalling firmHill-Rom, Inc.1069 State Road 46 E · Batesville, IN 47006-7520

✎ GovInfoNow plain-language explainer

Hill-Rom is recalling Progressa beds with catalog number P7500 that were made between May 12 and May 21, 2020. These beds have screws that may not meet strength requirements, which could cause serious injury to patients or users if the screw fails. Read more at govinfonow.com/recall/64876-hill-rom-progressa-bed-recall-screw-failure-risk-for-patient.

Source Summary by GovInfoNow · govinfonow.com/recall/64876-hill-rom-progressa-bed-recall-screw-failure-risk-for-patient · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2737-2020

Cite this page

“Hill-Rom Progressa Bed Recall: Screw Failure Risk for Patient Injury.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/64876-hill-rom-progressa-bed-recall-screw-failure-risk-for-patient. Based on FDA recall #Z-2737-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2737-2020%22&limit=1).

The FDA announced on June 30, 2020, that Hill-Rom, Inc. is recalling Progressa Beds due to screws that may not meet tensile strength requirements. Owners should contact the company for a remedy.

How to tell if you have it

Brand: Hill-Rom
Product: Progressa Bed
Catalog No.: P7500
Serial Numbers: V133AW9885 through V142AW0261
Manufacture Dates: May 12, 2020 to May 21, 2020

The hazard

Affected beds may have screws installed that do not meet material tensile strength requirements. Failure of this screw could result in serious patient or user injury.

Context

GovInfoNow's records show Hill-Rom, Inc. has 9 other recalls on record since January 12, 2018. Recent brand recalls include the Hill-Rom Traverse Rail Carriers recall on January 14, 2022, and the Hill-Rom Liko M220 Lifts recall on December 23, 2021. Other recent recalls of similar products include the Waldemar Link Endo-Model Plateau Recall (January 12, 2026), the Waldemar Link Endo-Model Replacement Plateau Recall (January 12, 2026), and the Genesis Screw-In Anchor Recall (December 17, 2025).

How to tell if you have this one

Check for Progressa Bed catalog number P7500 with serial numbers starting with V133AW9885 through V142AW0261. These beds were manufactured between May 12 and May 21, 2020.

Brand
Hill-Rom
Category
Medical device

FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class II
Status
Terminated
Distribution
Worldwide distribution - US nationwide distribution including in the states of AR, AZ, CA, DE, IN, KY, MD, ME, MI, MO, NC, NM, NY, OH, OK, PA, SC, TN, TX, VA, WA, WI, WV and the country of Canada.

Recall number	Product, codes & lots	Quantity
Z-2737-2020	Progressa Bed, Catalog No. P7500 - Product Usage: intended to be used to treat or prevent pulmonary or other complications associated with immobility; to treat or prevent pressure ulcers; or for any other use where medical benefits may be derived from either Continuous Lateral Rotation Therapy or Percussion/Vibration Therapy.; Serial Numbers Affected: V133AW9885 through V142AW0261and manufactured between May 12, 2020 and May 21, 2020	257
Z-2738-2020	Centrella Smart+ Bed, Catalog No. P7900 - Product Usage: intended to be used to treat or prevent pulmonary or other complications associated with immobility; to treat or prevent pressure ulcers; or for any other use where medical benefits may be derived from either Continuous Lateral Rotation Therapy or Percussion/Vibration Therapy.; Serial Numbers Affected: V133PF2502 through V142PF3819 and manufactured between May 12, 2020 and May 21, 2020	1033

Based on the official FDA remedy

What to do — step by step

Check Bed Serial Number
Look for the serial number on the bed's label to confirm if it falls within the affected range V133AW9885 to V142AW0261.
Contact Hill-Rom
Reach out to Hill-Rom directly for guidance on next steps if you have an affected bed.

Where it went and when

Where it was distributed

Distributed nationwide and abroad; the notice names 23 states.

FDA distribution: “Worldwide distribution - US nationwide distribution including in the states of AR, AZ, CA, DE, IN, KY, MD, ME, MI, MO, NC, NM, NY, OH, OK, PA, SC, TN, TX, VA, WA, WI, WV and the country of Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: Arizona, Arkansas, California, Delaware, Indiana, Kentucky, Maine, Maryland, Michigan, Missouri, New Mexico, New York, North Carolina, Ohio, Oklahoma, Pennsylvania, South Carolina, Tennessee, Texas, Virginia, Washington, West Virginia, Wisconsin.

Recall timeline

FDA terminated this recall 2.3 years after the firm started it.

Jun 30, 2020Firm started the recall
Jul 30, 2020FDA classified it Class II
Aug 5, 2020Published in FDA’s Enforcement Report
Oct 20, 2022FDA terminated the recall

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

Similar recalls

Latest medical device recalls

Keep exploring

More Hill-Rom recalls

Link to this recall

<a href="https://govinfonow.com/recall/64876-hill-rom-progressa-bed-recall-screw-failure-risk-for-patient">Hill-Rom Progressa Bed Recall: Screw Failure Risk for Patient Injury (GovInfoNow)</a>

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-2737-2020 (June 30, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2737-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.