FDA Adverse Event
Malfunction
Summary report: N
PROCEDURAL STRETCHER
MDR report key: 3173513
·
Received June 4, 2013
Report
- Report Number
- 3006697241-2013-00126
- Event Type
- Malfunction
- Date Received
- June 4, 2013
- Manufacturer
- HILLROM DE MEXICO S DE RL DE CV
- Product Code
- FPO
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
THE ACCOUNT FOUND THE SIDE RAIL ZERO TRANSFER STOP ARE CRACKED. THE ACCOUNT REPLACED THE SIDE RAIL ZERO TRANSFER STOPS TO RESOLVE THE ISSUE.
Description of Event or Problem · 1
(B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 247509 | PROCEDURAL STRETCHER | WHEELED STRETCHER | FPO | HILLROM DE MEXICO S DE RL DE CV |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |