FDA Adverse Event Malfunction Summary report: N

LD304 MATERNITY BED

MDR report key: 3201965 · Received July 2, 2013

Report

Report Number
0001831750-2013-05964
Event Type
Malfunction
Date Received
July 2, 2013
Date of Event
June 5, 2013
Report Date
June 5, 2013
Manufacturer
STRYKER MEDICAL-KALAMAZOO
Product Code
HDD
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

CONCLUSION: MANUFACTURER¿S INVESTIGATION IS STILL ONGOING; IF ADDITIONAL INFORMATION IS RECEIVED, A FOLLOW-UP REPORT WILL BE SUBMITTED.

Additional Manufacturer Narrative · 1

IT WAS INITIALLY REPORTED THAT THE FOOT SECTION HAD A BROKEN WELD WHICH MAY HAVE CAUSED THE CALF SUPPORT NOT TO LOCK INTO POSITION. FOLLOW-UP SUBMITTED AS FURTHER INVESTIGATION DETERMINED THE BROKEN FOOT SECTION WELD IS AN ANNOYANCE ISSUE ONLY. IT WAS CONFIRMED NO BED FUNCTIONS WERE AFFECTED AND NO SHARP EDGES WERE REPORTED. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED. THIS ISSUE IS NOT LIKELY TO CAUSE OR CONTRIBUTE TO SERIOUS INJURY OR DEATH IF IT WAS TO RECUR.

Description of Event or Problem · 1

IT WAS REPORTED VIA REPAIR WORK ORDER THAT THE FOOT SECTION HAD A BROKEN WELD WHICH MAY HAVE CAUSED THE CALF SUPPORT NOT TO LOCK INTO POSITION. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

Description of Event or Problem · 1

IT WAS REPORTED VIA REPAIR WORK ORDER THAT THE FOOT SECTION HAD A BROKEN WELD WHICH MAY HAVE CAUSED THE CALF SUPPORT NOT TO LOCK INTO POSITION. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
300709 LD304 MATERNITY BED TABLE, OBSTETRICAL, AC-POWERED (AND ACCESSORIES) HDD STRYKER MEDICAL-KALAMAZOO

Patients

Seq Age Sex Outcome Treatment
1