FDA Adverse Event Malfunction Summary report: N

M-1 COT - BASE HIGH LOAD 28

MDR report key: 1800585 · Received August 3, 2010

Report

Report Number
1831750-2010-01692
Event Type
Malfunction
Date Received
August 3, 2010
Date of Event
June 25, 2010
Report Date
July 7, 2010
Manufacturer
STRYKER CORP, MEDICAL DIV
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

ANY FURTHER INFORMATION FOUND TO BE RELEVANT TO THE INVESTIGATION WILL BE ADDED AND A FOLLOW UP MDR WILL BE SUBMITTED.

Description of Event or Problem · 1

IT HAS BEEN REPORTED THAT THE COT WAS ADJUSTED WITH THE FOOT END IN THE LAST NOTCH, THE HEAD END IN THE SECOND BUT LAST NOTCH. WHEN THE PATIENT WAS LYING IN THE COT, THE FOOT END SLID DOWN WITHOUT BEING TOUCHED BY THE PARAMEDICS. WHEN THE PARAMEDICS TRIED TO BRING THE COT BACK TO THE ABOVE DESCRIBED POSITION AND THEREFORE PULLED THE GRIP AT THE FOOT END OF THE LITTER, THE LITTER SLID ONE NOTCH DOWN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 M-1 COT - BASE HIGH LOAD 28 STRETCHER WHEELED FPO STRYKER CORP, MEDICAL DIV 6100 NA

Patients

Seq Age Sex Outcome Treatment
1 UNK