FMEA (Failure mode and effect analysis)
FMEA 
Introduction of FMEA (Failure mode and effect analysis)
FMEA is a preventative method used to identify potential ways in which a product or
process might not meet expectations. FMEA also aims to determine the effects of potential failures on the performance of the product/service or system. The process of ranking failure modes and causes may also be used to indicate where engineering effort should be concentrated to reduce failure occurrence.
Classifying the results of an FMEA in order of seriousness determines how critical the potential problems are.
According to Muhleman et al(1988), the primary objective of an FMEA is to determine the features of a service or product design and production/operations, which are critical to the various modes of failure. FMEA is most suitably applied at the design stage of a product or service to identify and eliminate failure causes. The technique draws all essential experience and information from design, marketing, production, purchasing and distribution to pinpoint the critical nature of potential problems and suggest action, which will assist in their prevention via FMEA.
According to Muhleman et al(1988) the core elements of FMEA are:
FMEA Element
FMEA Failure mode
The anticipated conditions of operation are used as the background to study the most probable failure mode, location and mechanism of the product/system and its components.
FMEA Failure effect
The potential failures are studied to determine their probable effects on the whole product/service and the effects of the various products on each other.
FMEA Failure criticality
The potential failures in the various parts of the product or service system are examined to determine the severity of each failure effect in terms of lowering performance, safety hazard, total loss of function etc.
Important steps in an FMEA analysis
The steps which should be considered when analysing FMEA include;
Identify the components of the product or system.
Identify all possible failure modes of each component..
Detail all the effects that each potential failure mode would have on the overall function of the product or system.
Identify all possible causes of each failure mode.
Assign numerical values to the failure modes on a scale of 1 to 10,(where 1 is low and 10 is high)for;
P = the probability of each failure mode occurring(1=low,10=high).
S = seriousness or criticality of the failure.
D = difficulty of detecting the failure before the product is used by the consumer.
These values may be represented in the form of a ratings table i.e. Calculate the Criticality index, C { C = SxPxD } for each failure mode in FMEA. This indicates the relative priority of each mode in the failure prevention activities and outline the corrective action required in FMEA.
Further features of FMEA
It may be observed that the FMEA technique is similar to QFD in that FMEA is also based on the completion of charts or matrices to identify problems and suggest relevant remedies. As QFD and FMEA charts must continuously be developed and updated, they are known as “live documents”. The major benefits of FMEA include the identification of weak points in the component or process under investigation and documentation of expert knowledge including:
Recording component functions.
Outlining production processes.
Collecting knowledge on failurs.
Carrying out the FMEA requires the co-operation of an inter-disciplinary team, due to the inter-departmental nature of the problems being examined. This process enhances the development of teamwork and employee involvement in an organisation, in keeping with the concepts of World Class Manufacturing.
The economic viability of the analysis must also be considered. The upkeep of FMEA requires a lot of clerical work and so it may be necessary to develop Corrective action software or FMEA software programs for the Business process management and displays of FMEA documentations(like AIAG FMEA, etc..).
Related articles by Zemanta
- Business Process Reengineeing (slideshare.net)
- 10th BPM Summit: Mastering Lean Six Sigma and Process Excellence (slideshare.net)
- Definiens AG Receives DIN EN ISO 9001:2008 and EN ISO 13485:2007 Certification (tissuepathology.typepad.com)

![Reblog this post [with Zemanta]](http://img.zemanta.com/reblog_e.png?x-id=49e8020a-978b-44fb-8462-611566abe5bc)







August 2nd, 2010 at 1:44 pm
Title…
I saw this really good website today….