Progressa® Bed System P7500ARecalls & reported problems

Summary

The FDA's MAUDE database contains 1,377 adverse event reports that list this exact device (DI 00887761000100), received between Mar 2, 2021 and Sep 30, 2026 — classified as 1 death, 44 injuries, 1,332 malfunctions.

The most frequently reported specific device problem is “Material Split, Cut or Torn” (1,013 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.

Recalls naming this device

1. Oct 18, 2022Open, Classified

   The compression links on impacted Progressa beds, listed in Appendix A, may bend when raising the head section. The labeling for these beds list a maximum patient weight of 500 lbs., however the bending may still occur with a patient weight of less than 500 lbs. depending on the patient 's position on the bed.

   Z-0231-2023 · Root cause: Under Investigation by firm · FDA record ↗

Most reported problems

Recent adverse event reports

The 25 most recent of 1,377 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 30, 2026Material Split, Cut or Torn

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50955198 ↗
• MalfunctionSep 28, 2026Unintended Movement

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50923801 ↗
• MalfunctionSep 25, 2026Material Split, Cut or Torn

  Baxter received a report stating that PROGRESSA FRAME power cord had copper wires exposed. This occurred during patient use. There was no patient or user injury, medical intervention, symptom, or adverse event reported.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50896732 ↗
• MalfunctionSep 24, 2026Material Split, Cut or Torn

  Baxter received a report stating that PROGRESSA FRAME auxiliary power cord had damage with exposed copper wires. This occurred before use. There was no patient/user injury, medical intervention, symptom, or adverse event reported.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50885815 ↗
• MalfunctionSep 24, 2026Material Frayed; Material Split, Cut or Torn

  Baxter received a report stating that PROGRESSA FRAME power cord had frayed damage with exposed copper wires. The process step at which the issue occurred was not specified. There was no patient/user injury, medical intervention, symptom, or adverse event reported.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50885583 ↗
• MalfunctionSep 24, 2026Material Split, Cut or Torn

  Baxter received a report that PROGRESSA FRAME had auxiliary power cord damaged with copper wire exposed. There was no patient/user injury, medical intervention, symptom, or adverse event reported.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50878037 ↗
• MalfunctionSep 23, 2026Material Split, Cut or Torn

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50875557 ↗
• MalfunctionSep 22, 2026Material Split, Cut or Torn

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50862576 ↗
• MalfunctionSep 22, 2026Material Split, Cut or Torn

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50859008 ↗
• MalfunctionSep 22, 2026Material Split, Cut or Torn

  Baxter received a report stating that PROGRESSA FRAME power cord had copper wires exposed. This occurred before use. There was no patient or user injury, medical intervention, symptom, or adverse event reported.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50855025 ↗
• MalfunctionSep 22, 2026Material Split, Cut or Torn

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50849375 ↗
• MalfunctionSep 21, 2026Material Split, Cut or Torn

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50849226 ↗
• MalfunctionSep 17, 2026Material Split, Cut or Torn

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50810911 ↗
• MalfunctionSep 17, 2026Material Split, Cut or Torn

  Baxter received a report that the PROGRESSA FRAME power cord had damage with exposed copper wires. The process step during which this occurred was unknown. There was no patient/user injury, medical intervention, symptom, or adverse event reported.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50804888 ↗
• MalfunctionSep 16, 2026Material Split, Cut or Torn

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50782501 ↗
• MalfunctionSep 15, 2026Unintended Movement

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50777255 ↗
• MalfunctionSep 15, 2026Material Split, Cut or Torn

  Baxter received a report that the PROGRESSA FRAME auxiliary cord has damage with copper conductor/ wires exposed. This occurred before use. There was no patient/user injury, medical intervention, symptom, or adverse event reported.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50774735 ↗
• MalfunctionSep 15, 2026Material Split, Cut or Torn

  Baxter received a report stating that PROGRESSA FRAME power cord had damage with exposed copper wires. This occurred during Baxter servicing/testing. There was no patient/user injury, medical intervention, symptom, or adverse event reported.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50773467 ↗
• MalfunctionSep 11, 2026Material Split, Cut or Torn

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50736851 ↗
• MalfunctionSep 11, 2026Material Split, Cut or Torn

  Baxter received a report that the PROGRESSA FRAME had damaged power cord, with copper wires exposed. The process step during which this occurred was unknown. There was no patient/user injury, medical intervention, symptom, or adverse event reported.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50736162 ↗
• MalfunctionSep 9, 2026Material Split, Cut or Torn

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50697419 ↗
• MalfunctionSep 9, 2026Material Split, Cut or Torn

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50696193 ↗
• MalfunctionSep 9, 2026Material Split, Cut or Torn

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50680732 ↗
• MalfunctionSep 8, 2026Material Split, Cut or Torn

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50680673 ↗
• MalfunctionSep 8, 2026Material Split, Cut or Torn

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50673400 ↗