EMT 480 Reliability & Failure Analysis
EMT 480 Reliability & Failure Analysis
EMT 480 Reliability & Failure Analysis
Failure
Analysis
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Benefits
Allows us to identify areas of our process that most
impact
our customers
Helps us identify how our process is most likely to fail
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Application Examples
Manufacturing: A manager is responsible for moving a
manufacturing operation to a new facility. He/she wants
to be sure the move goes as smoothly as possible and that
there are no surprises.
Design: A design engineer wants to think of all the a
possible ways product being designed could fail so that
robustness can be built into the product.
Software: A software engineer wants to think of possible problems
a software product could fail when scaled up to large
databases. This is a core issue for the Internet.
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What is Failure Mode and Effects
Analysis (FMEA)?
For electronic systems, FMEA is the common method
for
assessing and improving reliability based on failure
analysis.
Main objective of FMEA is to identify the potential
failure modes of the components contained in the
system under analysis
their consequences andfrequently
are, how their possible effects
they occur andon
how
the system
easily performance.
they can be detected.
It also aims to prioritise the failures according to how serious
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Examples
History of
FMEA
First used in the 1960’s in the Aerospace industry during
the Apollo missions
In 1974, the Navy developed MIL-STD-1629 regarding
the use of FMEA
In the late 1970’s, the automotive industry was by
driven
liability costs to use FMEA
Later, the automotive industry saw the
advantages of
using this tool to reduce risks related to poor quality
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What Can Go
Wrong?
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FMEA
Why
Methodology that facilitates process improvement
Identifies and eliminates concerns early in the of
development
a process or design
Improve internal and external customer satisfaction
Focuses on prevention
FMEA may be a customer requirement (likely
contractual)
FMEA may be required by an applicable
Quality Management System Standard (possibly
ISO)
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FME
A structured approach to:
A Identifying the ways in which a product or process
can fail
Estimating risk associated with specific causes
Prioritizing the actions
Evaluating design that
validation should
plan (designbeFMEA)
taken or
to current
reduce risk (process FMEA)
control plan
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When to Conduct an FMEA
Early in the process improvement investigation
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A Closer Look
Types of FMEAs
Design
Analyzes product design before release to
production, with a focus on product function
Analyzes systems and subsystems in early
concept and
design stages
Process
Used to analyze manufacturing and assembly processes
after they are implemented
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SYTEM – focuses on global system
function
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Process Steps
FMEA Procedure
1. For each process input (start with high value inputs), determine
the in which the input can go wrong (failure mode)
ways
2. failure mode, determine effects
For
Select a severity level for each effect (ie scratch, crack, contaminate etc)
each
3. Identify potential causes of each failure mode
Select an occurrence level for each cause (ie handling, machine
problem)
4.
List current controls for each cause
Select a detection level for each cause (ie provide training,
maintenance of the machine)
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Process Steps
FMEA Procedure
(Cont.)
5. Calculate the Risk Priority Number (RPN)
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Analyzing
and Detection
Severity
Importance of the effect on requirements
customer
Can be assigned from 1 (no danger) to 10 (critical)
Occurrence
The causes and frequencies of all possible failures from
(obtain past data if possible)
Can be assigned from 1 (low) to10 (extremely high)
Detection
The ability of the current control scheme to detect
(then prevent) for a given cause (may be difficult to estimate
early in process operations).
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Calculating a
Composite
Score
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It is the name of the component which is analyzed
Identifies the name and ID of the systems or
subsystems
Contains names of the responsible individuals that
have the authority to perform task
Identifies the team responsible for this design
Used for document tracking purposes
Contains the original date and revised date
Contains the name and Id of item being analyzed as
well as one specific function of the item
Contains methods
1.May fail to meet design criteria
2.May cause potential failure in high level systems
and low level system
Severity(S)
Used to specify any additional controls
Reasons for failure
Occurrence(O)
Prevention measures
Risk priority number(RPN)=S*O*D
Corrective actions examined by the team
Target completion dates
After an action has been taken, the actual action
and the effective date should be entered in this
colums
Key Points
Summary
An FMEA:
Identifies the ways in which a product or fail
process can
Estimatesthethe
Prioritizes risk associated
actions with
that should be specific
taken to reduce risk
causes
FMEA is a team tool
There are two different types of FMEAs:
Design
Process
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