FDA Adverse Event
Injury
Summary report: N
SUNSET 25FT OXYGEN SUPPLY TUBE - GREEN
MDR report key: 24613087
·
Received March 16, 2026
Report
- Report Number
- 3006446479-2026-00001
- Event Type
- Injury
- Date Received
- March 16, 2026
- Date of Event
- January 18, 2026
- Report Date
- March 16, 2026
- Manufacturer
- NINGBO RUNMAI MEDICAL TECHNOLOGY CO., LTD.
- Product Code
- BYX
- UDI-DI
- 00848530061081
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- 501
Narratives
Additional Manufacturer Narrative · 0
N/A.
Description of Event or Problem · 0
ON 02/16/2026, SUNSET HEALTHCARE SOLUTIONS RECEIVED AN FDA MEDWATCH REPORT THAT A VITAS HEALTHCARE PATIENT ALLEGEDLY TRIPPED ON OUR RES3025G OXYGEN SUPPLY TUBING WHILE WALKING TO OPEN HER DOOR. IT WAS STATED THAT SHE LOST HER BALANCE AND FELL FORWARD, RESULTING IN A HIP FRACTURE REQUIRING SURGERY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 664735 | SUNSET 25FT OXYGEN SUPPLY TUBE - GREEN | OXYGEN SUPPLY TUBE | BYX | NINGBO RUNMAI MEDICAL TECHNOLOGY CO., LTD. | RES3025G | NOT REPORTED | 00848530061081 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 82 YR | Female | Hospitalization | 5L OXYGEN CONCENTRATOR| NEBULIZER| PORTABLE OXYGEN CONCENTRATOR |