inforMED
MalfunctionIOQ

TOTALCARE BED

Received May 8, 2026 · Event occurred Apr 13, 2026

Report 1824206-2026-01020 · MDR key 25129014

Device

Generic name

Bed, Flotation Therapy, Powered

Model number

P1900M

Catalog number

P1900M

Product problems

  • Positioning Failure

Patient

NA · Unknown

  • No Clinical Signs, Symptoms or Conditions

Narrative

Additional Manufacturer Narrative

BAXTER HAS CONTACTED THE ACCOUNT THREE TIMES REQUESTING THE DEVICE TO BE RETURNED FOR INSPECTION. THE ACCOUNT WAS UNRESPONSIVE TO THE ATTEMPTS AND THE DEVICE DID NOT RETURN TO MANUFACTURE. THEREFORE, BAXTER IS COMPLETING THIS COMPLAINT DUE TO THE AMOUNT OF TIME. BASED ON THIS INFORMATION, NO FURTHER ACTION IS REQUIRED. PER THE BAXTER SERVICE MANUAL THE TOTALCARE BED SYSTEM REQUIRES AN EFFECTIVE MAINTENANCE PROGRAM. WE RECOMMEND THAT YOU PERFORM A SEMI-ANNUAL PREVENTATIVE MAINTENANCE. PREVENTATIVE MAINTENANCE WILL MINIMIZE DOWNTIME DUE TO EXCESSIVE WEAR. TEST THE HEAD SECTION SLIDE PIVOTS, SELF-LUBRICATING BEARING, AND SLIDER PIVOT EXTRUSIONS. LOOK FOR DAMAGE, AND MAKE SURE THE HEAD SECTION OPERATES CORRECTLY. REPLACE COMPONENTS AS NECESSARY.

Description of Event or Problem

BAXTER RECEIVED A REPORT THAT TOTALCARE PRODUCT CONFIG HAD HEAD NOT GOING UP. THE PROCESS STEP DURING WHICH THIS OCCURRED WAS UNKNOWN. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.