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