FDA Adverse Event
Injury
Summary report: N
STRYKER, CUB
MDR report key: 3060131
·
Received April 9, 2013
Report
- Report Number
- MW5029739
- Event Type
- Injury
- Date Received
- April 9, 2013
- Date of Event
- April 4, 2013
- Report Date
- April 9, 2013
- Manufacturer
- UNK
- Product Code
- FMS
- Adverse Event
- Yes
- Report Source
- Voluntary report
- Reporter Location
- CA, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
STAFF FOUND PT IN THE CRIB WITH LEFT LEG CAUGHT IN BETWEEN THE RAILS. THE PT WAS STRUGGLING TO TAKE HIS LEFT LEG OUT. PT APPEARED TO BE IN PAIN. UPON ASSESSMENT NOTICED SLIGHT SWELLING AND INDURATION BELOW LEFT LATERAL ASPECT OF THE KNEE. THERE WAS NO FRACTURE AND THERE WAS NO PERMANENT INJURY SUSTAINED. THIS EQUIPMENT WAS RENTED BY FACILITY THROUGH UNIVERSAL HOSPITAL SUPPLY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 144465 | STRYKER, CUB | CRIB BED | FMS | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 25 MO |