Progressa+ Bed P7501ARecalls & reported problems

Summary

The FDA's MAUDE database contains 36 adverse event reports that list this exact device (DI 00887761966925), received between Aug 23, 2024 and Sep 9, 2026 — classified as 2 injuries, 34 malfunctions.

The most frequently reported specific device problem is “Material Split, Cut or Torn” (25 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 4, 2023Open, Classified

   Progressa+ beds have the potential for static buildup from the casters and/or power drive. This static electricity could be passed to the operator through the transport handle during transport, resulting in a mild static electric shock.

   Z-0212-2024 · Root cause: Under Investigation by firm · FDA record ↗

Most reported problems

Recent adverse event reports

The 25 most recent of 36 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 9, 2026Material Split, Cut or Torn

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50702840 ↗
• MalfunctionSep 4, 2026Unintended Movement

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50615708 ↗
• MalfunctionAug 31, 2026Unintended Movement

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50532324 ↗
• MalfunctionAug 12, 2026Material Split, Cut or Torn

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50225519 ↗
• MalfunctionJul 27, 2026Unintended Movement

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50037659 ↗
• MalfunctionJul 17, 2026Unintended Movement

  BAXTER RECEIVED A REPORT THAT PROGRESSA PLUS HAD BRAKES NOT HOLDING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25861711 ↗
• MalfunctionApr 17, 2026Material Split, Cut or Torn

  BAXTER RECEIVED A REPORT THAT PROGRESSA PLUS HAD THE 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 24912312 ↗
• MalfunctionMar 11, 2026Material Split, Cut or Torn

  ON 11-FEB-2026, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT PROGRESSA PLUS (PRODUCT CODE P7501A000032, SERIAL NUMBER (B)(6)), HAD 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 24573415 ↗
• MalfunctionMar 6, 2026Collapse

  ON 09-FEB-2026, A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT PROGRESSA PLUS (PRODUCT CODE P7501A000095, SERIAL NUMBER (B)(6)), HAD SIDERAIL WAS BROKEN AND FALLING OFF. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24532853 ↗
• MalfunctionFeb 24, 2026Material Split, Cut or Torn

  ON 29-JAN-2026, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT PROGRESSA PLUS (PRODUCT CODE P7501A000032, SERIAL NUMBER (B)(6)), HAD AUXILIARY POWER CORD DAMAGED WITH COPPER 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 24431730 ↗
• InjuryFeb 24, 2026Improper Flow or Infusion

  IT WAS REPORTED PROGRESSA PLUS BED HAD AN ACB (AIR CONTROL BOARD) ERROR FAULT CAUSING THE MATTRESS TO DEFLATE WHICH RESULTED IN THE PATIENT SUSTAINING A DEEP TISSUE PRESSURE INJURY. THE PATIENT RECEIVED UNSPECIFIED ¿WOUND CARE TREATMENT.¿ MULTIPLE ATTEMPTS WERE MADE TO THE CUSTOMER TO OBTAIN SPECIFIC DETAILS OF THE REPORTED DEEP TISSUE PRESSURE INJURY, INCLUDING LOCATION, CHARACTERISTICS, AND WHAT MEDICAL INTERVENTION WAS PERFORMED, HOWEVER NO RESPONSE WAS RECEIVED. AN INSPECTION PERFORMED BY A BAXTER TECHNICIAN NOTED THE SUPPLY HOSE HAD DISCONNECTED. THE TECHNICIAN RECONNECTED THE SUPPLY HOSE AND NOTED THE BED WAS FUNCTIONING AS DESIGNED. NO FURTHER INFORMATION WAS AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Unspecified Tissue Injury

  MAUDE report 24431622 ↗
• MalfunctionFeb 11, 2026No Audible Alarm

  ON 14-JAN-2026, A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT PROGRESSA PLUS (PRODUCT CODE P7501A000032, SERIAL NUMBER (B)(6)), HAD BED EXIT NOT SENDING SIGNAL TO NURSE CALL. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24314597 ↗
• MalfunctionFeb 3, 2026Material Split, Cut or Torn

  ON (B)(6) 2026, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT PROGRESSA PLUS (PRODUCT CODE P7501A000032, SERIAL NUMBER (B)(6) , HAD AUXILIARY POWER CORD DAMAGED WITH COPPER 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 24248467 ↗
• MalfunctionJan 21, 2026Material Split, Cut or Torn

  ON 06-JAN-2026, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT PROGRESSA PLUS (PRODUCT CODE P7501A000033, SERIAL NUMBER (B)(6)), HAD AUXILIARY POWER CORD DAMAGED 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 24134074 ↗
• MalfunctionJan 15, 2026Flare or Flash

  ON 30-DEC-2025, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT PROGRESSA PLUS (PRODUCT CODE P7501A000191, SERIAL NUMBER (B)(6)), A FIRE WAS OBSERVED INVOLVING THE POWER CORD. THIS OCCURRED DURING PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24083772 ↗
• MalfunctionJan 7, 2026Material Split, Cut or Torn

  ON 31-DEC-2025, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT PROGRESSA PLUS (PRODUCT CODE P7501A000032, SERIAL NUMBER (B)(6)), HAD AUXILIARY POWER CORD DAMAGED WITH COPPER 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 23998115 ↗
• MalfunctionJan 7, 2026Material Split, Cut or Torn

  ON (B)(6) 2025, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT PROGRESSA PLUS (PRODUCT CODE P7501A000032, SERIAL NUMBER (B)(6)), HAD AUXILIARY POWER CORD DAMAGED WITH COPPER 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 23995594 ↗
• MalfunctionNov 6, 2025Material Split, Cut or Torn; Material Split, Cut or Torn

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN TO REPORT THE PROGRESSA PLUS AUXILIARY POWER CORD HAD COPPER WIRES EXPOSED. THE BED WAS LOCATED AT THE ACCOUNT. THIS OCCURRED AFTER PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. IT WAS UNKNOWN IF ANY SECOND DEVICE WAS ALSO INVOLVED. THE CUSTOMER DID NOT KNOW IF THIS EVENT WAS ALREADY COMMUNICATED TO ANOTHER BAXTER DEPARTMENT OR AUTHORITY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23486992 ↗
• MalfunctionNov 4, 2025Material Split, Cut or Torn; Material Split, Cut or Torn

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN TO REPORT THE PROGRESSA PLUS AUXILIARY POWER CORD HAD COPPER WIRES EXPOSED. THE BED WAS LOCATED AT THE ACCOUNT. THIS OCCURRED AFTER PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. IT WAS UNKNOWN IF ANY SECOND DEVICE WAS ALSO INVOLVED. THE CUSTOMER DID NOT KNOW IF THIS EVENT WAS ALREADY COMMUNICATED TO ANOTHER BAXTER DEPARTMENT OR AUTHORITY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23466351 ↗
• MalfunctionNov 3, 2025Material Split, Cut or Torn; Material Split, Cut or Torn

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN TO REPORT THE PROGRESSA PLUS AUXILIARY POWER CORD HAD COPPER WIRES EXPOSED. THE BED WAS LOCATED AT THE ACCOUNT. THE PROCESS STEP DURING WHICH THIS OCCURRED WAS UNKNOWN. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE CUSTOMER DID NOT KNOW IF THIS EVENT WAS ALREADY COMMUNICATED TO ANOTHER BAXTER DEPARTMENT OR AUTHORITY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23458760 ↗
• MalfunctionNov 3, 2025Material Split, Cut or Torn; Material Split, Cut or Torn

  ON 10-OCT-2025, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT PROGRESSA PLUS (PRODUCT CODE P7501A001971, (B)(6), HAD POWER CORD DAMAGED WITH EXPOSED COPPER WIRES. THIS OCCURRED AFTER PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23458245 ↗
• MalfunctionOct 30, 2025Activation Problem; Activation Problem

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN STATING THE CPR FUNCTION WAS INOPERATIVE . THE BED WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT/USER INJURY REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23426012 ↗
• MalfunctionOct 15, 2025Material Split, Cut or Torn; Material Split, Cut or Torn

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN STATING THE AUX CORD HAD DAMAGE WITH EXPOSED COPPER WIRES. THE BED WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT/USER INJURY REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23286593 ↗
• MalfunctionAug 27, 2025Material Split, Cut or Torn; Material Split, Cut or Torn

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN TO REPORT THE PROGRESSA PLUS AUXILIARY POWER CORD HAD COPPER WIRES EXPOSED. THE BED WAS LOCATED AT THE ACCOUNT. THIS OCCURRED BEFORE USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE CUSTOMER DID NOT COMMUNICATE THIS EVENT TO ANOTHER BAXTER DEPARTMENT OR AUTHORITY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22907828 ↗
• MalfunctionAug 21, 2025Material Split, Cut or Torn; Material Split, Cut or Torn

  BAXTER RECEIVED A REPORT STATING THAT PROGRESSA PLUS AUXILIARY POWER CORD HAD DAMAGE WITH EXPOSED COPPER WIRES. THE BED WAS LOCATED AT THE ACCOUNT AND OCCURRED AFTER PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22861712 ↗