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Progressa® Surface P7520A23Recalls & reported problems

Hill-Rom, Inc. · Hospital Bed Surface · Class 2

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
4
Deaths reported
0
Injuries reported
4
Recalls naming it
1

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00887761999855), received between Feb 4, 2025 and Feb 10, 2025 — classified as 4 injuries.

The most frequently reported specific device problem is “Material Twisted/Bent” (3 reports).

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 4 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520264
Last 36 months. The most recent month may be incomplete.

Recalls naming this device

  1. Feb 25, 2025Open, Classified

    The air bladders inside the mattress may move out of position when the head of the bed is elevated, causing a dip in the mattress.

    Z-1468-2025 · Root cause: Nonconforming Material/Component · FDA record ↗

Most reported problems

Device problems

  • Material Twisted/Bent3
  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Pressure Sore/Ulcer4

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

  • InjuryFeb 10, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED BY THE CUSTOMER THE BLADDER IN A PROGRESSA BED SURFACE WAS TWISTING AND CAUSING A DIP, AND A PATIENT INJURY OCCURRED. FORTY TWO DAYS PRIOR TO THIS REPORT, THE PATIENT DEVELOPED A DEEP TISSUE PRESSURE INJURY (DTPI) TO THE LEFT SACRUM/BUTTOCK. ON AN UNKNOWN DATE, THE PATIENT WAS ADMITTED TO THE HOSPITAL FOR AN UNSPECIFIED DIAGNOSIS AND PLACED ON A PROGRESSA BED. AFTER AN UNSPECIFIED AMOUNT OF TIME, THE DTPI "WORSENED". THE PATIENT UNDERWENT A DEBRIDEMENT OF THE WOUND. AT THE TIME OF THIS REPORT, THE WOUND WAS CONSIDERED A STAGE 4 DTPI. NO FURTHER INFORMATION WAS AVAILABLE AT THE TIME OF THIS REPORT.

    Patient problems: Pressure Sore/Ulcer

    MAUDE report 21349635 ↗
  • InjuryFeb 4, 2025Material Twisted/Bent; Material Twisted/Bent

    IT WAS REPORTED BY THE CUSTOMER THE BLADDER IN A PROGRESSA BED SURFACE WAS TWISTING AND CAUSING A DIP, AND A PATIENT INJURY OCCURRED. DURING AN ONSITE VISIT BY BAXTER TEAM MEMBERS THE CUSTOMER REPORTED ON AN UNKNOWN DATE, THE PATIENT WAS ADMITTED TO THE HOSPITAL FOR AN UNSPECIFIED DIAGNOSIS. DURING HOSPITALIZATION WHILE USING THE PROGRESSA BED THE PATIENT DEVELOPED A DEEP TISSUE PRESSURE INJURY (DTPI) CONSIDERED A STAGE 4 WOUND BASED ON THE RIGHT ISCHIUM. THE PATIENT WAS TREATED WITH A ¿TOPICAL¿ WOUND CARE (NOT FURTHER SPECIFIED). NO FURTHER INFORMATION WAS AVAILABLE AT THE TIME OF THIS REPORT.

    Patient problems: Pressure Sore/Ulcer

    MAUDE report 21304945 ↗
  • InjuryFeb 4, 2025Material Twisted/Bent; Material Twisted/Bent

    IT WAS REPORTED BY THE CUSTOMER THE BLADDER IN A PROGRESSA BED SURFACE WAS TWISTING AND CAUSING A DIP, AND A PATIENT INJURY OCCURRED. DURING AN ONSITE VISIT BY BAXTER TEAM MEMBERS THE CUSTOMER REPORTED THE PATIENT HAD AN INITIAL STAGE 4 PRESSURE SORE ON THE RIGHT SACRUM. THEN ON AN UNKNOWN DATE, THIS PATIENT WAS ADMITTED TO THE HOSPITAL FOR AN UNSPECIFIED DIAGNOSIS. ON THE DATE OF THE EVENT, THE STAGE 4 PRESSURE INJURY WAS OBSERVED TO HAVE ¿WORSENED¿. ALSO ON THIS DATE, WHILE HOSPITALIZED, THE PATIENT DEVELOPED A STAGE 4 PRESSURE INJURY ON THE LEFT SACRUM. THE PATIENT UNDERWENT A DEBRIDEMENT TO BOTH PRESSURE INJURIES. THE PATIENT LATER RECOVERED FROM THE STAGE 4 PRESSURE INJURY LEAVING THE PATIENT WITH THE INITIAL STAGE 4 PRESSURE INJURY THEY WERE ADMITTED TO THE HOSPITAL WITH. THE CUSTOMER REPORTED A NON-BAXTER MAPPING PAD WAS USED ON THE PROGRESSA BED SURFACE BETWEEN THE MICROCLIMATE MANAGEMENT (MCM) TOPPER AND THE AIR BLADDERS. ON AN UNKNOWN DATE, THE CUSTOMER REPLACED THE MATTRESS. NO FURTHER INFORMATION WAS AVAILABLE AT THE TIME OF THIS REPORT.

    Patient problems: Pressure Sore/Ulcer

    MAUDE report 21304935 ↗
  • InjuryFeb 4, 2025Material Twisted/Bent; Material Twisted/Bent

    IT WAS REPORTED BY THE CUSTOMER THE BLADDER IN A PROGRESSA BED SURFACE WAS TWISTING AND CAUSING A DIP, AND A PATIENT INJURY OCCURRED. DURING AN ONSITE VISIT BY BAXTER TEAM MEMBERS THE CUSTOMER REPORTED THE PATIENT HAD AN INITIAL STAGE 4 PRESSURE SORE ON THE SACRUM. THEN ON AN UNKNOWN DATE, THIS PATIENT WAS ADMITTED TO THE HOSPITAL FOR AN UNSPECIFIED DIAGNOSIS. ON THE DATE OF THE EVENT, A DEEP TISSUE PRESSURE INJURY (DTPI) DEVELOPED INSIDE THE PREEXISTING STAGE 4 WOUND. NO MEDICAL INTERVENTION WAS PROVIDED. THE PROGRESS BED WAS REPLACED, AND THE PATIENT DEVELOPED A SECOND DTPI. NO MEDICAL INTERVENTION WAS PROVIDED FOR THIS INJURY AS WELL. NO FURTHER INFORMATION WAS AVAILABLE AT THE TIME OF THIS REPORT.

    Patient problems: Pressure Sore/Ulcer

    MAUDE report 21304053 ↗

Other BED, AC-POWERED ADJUSTABLE HOSPITAL devices

All BED, AC-POWERED ADJUSTABLE HOSPITAL devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.