pro+ P7924ARENT01Recalls & reported problems

Summary

The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI 00887761976863), received between Dec 19, 2023 and Aug 11, 2026 — classified as 1 death, 14 malfunctions.

The most frequently reported specific device problem is “Material Split, Cut or Torn” (14 reports).

3 FDA recall records name this device's identifier, 3 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. May 8, 2024Open, Classified

   There is a potential for the top cover of the hospital bed mattress to delaminate as a result of improper cleaning and lack of adequate details on the appropriate use of cleaning agents containing bleach.

   Z-2151-2024 · Root cause: Error in labeling · FDA record ↗

2. Mar 31, 2023Open, Classified

   There is a potential for mattress cover damage (delamination) which may result in fluid absorption in the mattress (fluid ingress).

   Z-1482-2023 · Root cause: Process change control · FDA record ↗

3. Jun 24, 2022Open, Classified

   The failure mode on the affected mattresses can cause a reduction in the performance of the Microclimate Management feature used to pull heat and moisture away from the patient resulting in an increased patient risk of pressure ulcer development.

   Z-1411-2022 · Root cause: Nonconforming Material/Component · FDA record ↗

Most reported problems

Recent adverse event reports

The 15 most recent of 15 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 11, 2026Material Split, Cut or Torn

  Baxter received a report that FLAT DECK 36" MRS W/ X-RAY SLV 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 50204258 ↗
• DeathMay 20, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THERE WAS NO AIR RUNNING THROUGH THE PRO+ AND THE PATIENTS¿ PRESSURE WOUNDS WERE GETTING WORSE. THE CUSTOMER REPORTED THE LOCATION OF THE PRESSURE SORES WERE ALONG HIS SPINE FROM HIS MID-UPPER BACK DOWN TO HIS COCCYX AND STATED THEY WERE UNSTAGEABLE DEEP TISSUE. THE CUSTOMER WAS UNABLE TO PROVIDE THE STAGING OF THE PRESSURE WOUNDS PRIOR TO THEM GETTING WORSE. THE CUSTOMER REPORTED THAT A TURN SCHEDULE WAS IMPLEMENTED AND THEN THEY STARTED TO USE A DRESSING, CUSTOMER DID NOT REMEMBER THE NAME BUT STATED "IT WAS LIKE AQUACEL." THE PATIENT WAS TRANSFERRED TO A HIGHER LEVEL OF CARE, AFTER THIS THE PATIENT PASSED AWAY (DATE UNKNOWN). THE CUSTOMER NOTED ON ADMISSION THE PATIENT WAS "EXTREMELY DECLINED AND WAS UNABLE TO GET OUT OF BED". IT IS UNKNOWN WHEN THE PATIENT DIED OR THE CAUSE OF DEATH. IT WAS NOT REPORTED IF AN AUTOPSY WAS PERFORMED. A BAXTER TECHNICIAN INSPECTED THE BED AND WAS UNABLE TO DUPLICATE ANY ISSUES. THE TECHNICIAN FOUND THE BED TO BE FUNCTIONING AS DESIGNED. NO FURTHER INFORMATION WAS AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Unspecified Tissue Injury

  MAUDE report 25232663 ↗
• MalfunctionMay 4, 2026Material Split, Cut or Torn

  A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT FLAT DECK 36" MRS W/ X-RAY SLV HAD AN ISSUE, POWER CORD IS CUT IN HALF. USER DEFINED DESCRIPTION: WAREHOUSE REPAIR. 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 25070897 ↗
• MalfunctionApr 14, 2026Material Split, Cut or Torn

  A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT FLAT DECK 36" MRS W/ X-RAY SLV HAD AN ISSUE, FRAYED POWER CORD (EXPOSED COPPER). THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24879204 ↗
• MalfunctionFeb 26, 2026Material Split, Cut or Torn

  ON (B)(6) 2026, DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT FLAT DECK 36" MRS W/ X-RAY SLV (PRODUCT CODE P7924ARENT01, SERIAL NUMBER (B)(6)), HAD POWER CORD DAMAGED WITH COPPER WIRES EXPOSED. 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 24463888 ↗
• MalfunctionJun 10, 2025Material Split, Cut or Torn; Material Split, Cut or Torn

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN STATING THE POWER 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 22177846 ↗
• MalfunctionMay 23, 2025Material Split, Cut or Torn; Material Split, Cut or Torn

  IT WAS REPORTED THAT FLAT DECK 36" MRS W/ X-RAY SLV (PRODUCT CODE P7924ARENT01, SERIAL NUMBER (B)(6)), HAD POWER CORD 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 22080476 ↗
• MalfunctionFeb 18, 2025Material Split, Cut or Torn; Material Split, Cut or Torn

  IT WAS REPORTED THAT FLAT DECK 36" MRS W/ X-RAY SLV (PRODUCT CODE P7924ARENT01, SERIAL NUMBER (B)(6)), HAD POWER CORD DAMAGE 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 21397546 ↗
• MalfunctionFeb 12, 2025Material Split, Cut or Torn; Material Split, Cut or Torn

  IT WAS REPORTED THAT FLAT DECK 36" MRS W/ X-RAY SLV (PRODUCT CODE P7924ARENT01, SERIAL NUMBER (B)(6), HAD THE POWER CORD 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 21366467 ↗
• MalfunctionSep 20, 2024Material Split, Cut or Torn; Material Split, Cut or Torn

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN STATING THE POWER CORD HAD DAMAGE WITH EXPOSED COPPER WIRES. THE BED WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT/USER INJURY REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20267779 ↗
• MalfunctionAug 9, 2024Material Split, Cut or Torn; Material Split, Cut or Torn

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN STATING THE POWER CORD HAD DAMAGE WITH EXPOSED COPPER WIRES. THE BED WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT/USER INJURY REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19954961 ↗
• MalfunctionMay 23, 2024Material Split, Cut or Torn; Material Split, Cut or Torn

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN STATING THE POWER CORD HAD DAMAGE WITH EXPOSED COPPER WIRES. THE BED WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT/USER INJURY REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19385703 ↗
• MalfunctionMay 10, 2024Material Split, Cut or Torn; Material Split, Cut or Torn

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN STATING THE POWER CORD HAD DAMAGE WITH EXPOSED COPPER WIRES. THERE WAS NO PATIENT/USER INJURY REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19284357 ↗
• MalfunctionApr 9, 2024Material Split, Cut or Torn; Material Split, Cut or Torn

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN STATING THE POWER CORD HAD DAMAGE WITH EXPOSED COPPER WIRES. THE BED WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT/USER INJURY REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT (B)(4) .

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19075456 ↗
• MalfunctionDec 19, 2023Material Split, Cut or Torn; Material Split, Cut or Torn

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN STATING THE BED HAD POWER CORD DAMAGE WITH EXPOSED COPPER WIRES. THE BED WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT/USER INJURY REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT #: (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18356407 ↗