VERSACARE MED SURG BED
Report
- Report Number
- 1824206-2026-01251
- Event Type
- Malfunction
- Date Received
- May 29, 2026
- Date of Event
- May 6, 2026
- Report Date
- May 29, 2026
- Manufacturer
- BAXTER HEALTHCARE CORPORATION
- Product Code
- FNL
- UDI-DI
- 00887761000872
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- OTHER
Narratives
THE BAXTER TECHNICIAN FOUND THE POWER CORD NEEDED TO BE REPLACED. A SEARCH OF THE BAXTER MAINTENANCE RECORDS SHOWED BAXTER PERFORMED PREVENTATIVE MAINTENANCE ON THIS BED IN NOV 14, 2025. IT IS UNKNOWN IF THE FACILITY PERFORMED ANY OTHER PREVENTATIVE MAINTENANCE ON THIS BED. PER THE BAXTER SERVICE MANUAL, PERFORM ANNUAL PREVENTIVE MAINTENANCE PROCEDURES TO MAKE SURE ALL VERSACARE BED COMPONENTS ARE FUNCTIONING AS ORIGINALLY DESIGNED. EXAMINE THE PLUG FOR DAMAGE. MAKE SURE THE PLUG IS A ONE-PIECE MOLDED PLUG ASSEMBLY. IF IT IS NOT, REPLACE THE PLUG CORD ASSEMBLY. REPLACE ANY PLUG CORD ASSEMBLY THAT SHOWS ANY OF THESE: DISCOLORATION OF THE PLUG MOLDING, AROUND THE PLUG BLADES. ANY SIGNS OF CRACKING., LOOSE FIT OF THE PLUG BLADE (THE PLUG BLADE MOVES IN THE MOLDING), VERIFY THAT THE STRAIN RELIEF P-CLIP IS PRESENT. REPLACE THE POWER CORD, IF DAMAGED. THE TECHNICIAN REPLACED THE POWER CORD TO RESOLVE THE REPORTED EVENT. BASED ON THIS INFORMATION, NO FURTHER ACTION IS REQUIRED.
BAXTER RECEIVED A REPORT THAT VERSACARE FRAME HAD POWER CORD DAMAGED WITH COPPER WIRE EXPOSED. THIS OCCURRED DURING BAXTER SERVICING/TESTING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 130687 | VERSACARE MED SURG BED | BED, AC-POWERED ADJUSTABLE HOSPITAL | FNL | BAXTER HEALTHCARE CORPORATION | P3200K | 00887761000872 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |