FDA Adverse Event Other Summary report: N

2432235-2010-00191

MDR report key: 1932236 · Received December 10, 2010

Report

Report Number
2432235-2010-00191
Event Type
Other
Date Received
December 10, 2010
Date of Event
November 10, 2010
Report Date
November 10, 2010
Manufacturer
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD.
PMA / PMN Number
K970227
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Patients

Seq Age Sex Outcome Treatment
1 NA Female