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FMEA. Failure Mode Effect Analysis

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FMEA

Failure Mode Effect Analysis

FMEA

Failure Mode Effect Analysis

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FMEA

• Failure Mode and Effect Analysis is also known as risk analysis.

• It is a preventive measure to systematically display the causes, effects and possible actions regarding observed failures.

• Is an engineering technique used to define, identify and eliminate known or potential failures, problem, errors.

• It is before-the-event action

• Is a never ending process improvement tool.

Failure Mode and Effect Analysis is also known as risk analysis.

It is a preventive measure to systematically display the causes, effects and possible actions regarding observed failures.

Is an engineering technique used to define, identify and eliminate known or potential failures, problem, errors.

Is a never ending process improvement tool.

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FMEA - OBJECTIVES

1. Find failures and prevent them.

2. Priorities failures and attempts to eliminate them.Priorities failures and attempts to eliminate them.

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TYPES OF FMEA

1. System FMEA -

2. Design FMEA -

3. Process FMEA -

4. Service FMEA -

5. Equipment FMEA -

6. Maintenance FMEA -

7. Concept FMEA -

8. Environmental FMEA -

Design FMEA

Process FMEA

Design FMEA Process FMEA

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BENEFITS OF FMEA

1. Improve product/process reliability and quality.

2. Increase customer satisfaction.

3. Early identification/elimination of failure modes.

4. Prioritize product/process deficiencies.

5. Capture engineering/organisation knowledge

6. Document and track the action taken to reduce risk 7. Focus for improved testing and development

8. Act as catalyst.

Improve product/process reliability and quality.

Early identification/elimination of failure modes.

Prioritize product/process deficiencies.

Capture engineering/organisation knowledge

Document and track the action taken to reduce risk Focus for improved testing and development

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INPUTS FOR FMEA

1. People inputs: FMEA is a team work. The team should have assembly engineer, manufacturing engineer, material engineer, quality engineer, service engineer, suppliers and the customer.

■ 2. Data inputs: Product and process specifications, reliability data,

customer priority data, process variability data, process descriptions and inspection data.

FMEA is a team work. The team should have assembly engineer, manufacturing engineer, material engineer, quality engineer, service engineer, suppliers and the customer.

Product and process specifications, reliability data,

customer priority data, process variability data, process descriptions and

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STAGES OF FMEA

Stage 1: Specifying Possibilities i) Functions

ii) ii) Possible failure mode iii) iii) Root causes

iv) Effects

v) Detection/Prevention.

Stage 2: Quantifying Risks i) Probability of cause

ii) ii) Severity of effect

iii) Effectiveness of control to prevent cause

iv) Risk Priority Number (RPN)

iii) Effectiveness of control to prevent cause

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STAGES OF FMEA

■ Stage 3: Correcting High Risk Causes i) Prioritizing work

ii) Detailing action

iii) Assigning action responsibility iv) Check points on completion

■ Stage 4: Re-evaluation of Risk

■ i) Recalculation of risk priority number Stage 3: Correcting High Risk Causes

) Recalculation of risk priority number

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FMEA PROCEDURE

1. Describe the product/process and its function 2. Create a block diagram of the product/process

3. Complete the header of the FMEA form worksheet 4. List product/process functions

5. Identify failure modes

failure mode includes corrosion failure, fatigue, deformation, cracking, electrical short or open etc..

6. Describe the potential failure effects

defined as the result of a failure mode on the function of the product/process

ex: injury to the user, impaired operation, poor appearance, odour, noise etc..

Describe the product/process and its function Create a block diagram of the product/process

Complete the header of the FMEA form worksheet

failure mode includes corrosion failure, fatigue, deformation, cracking,

defined as the result of a failure mode on the function of the

ex: injury to the user, impaired operation, poor appearance, odour, noise

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FMEA PROCEDURE

7. Establish a numerical ranking for the Severity(S) of the effect

S is the assessment of the seriousness of the failure effect

standard scale uses 1 for no effect and 10 for very serious effect.

8. The CLASS column is filled

Used to classify any special product characteristics for components that may require additional process controls.

9. Identify the potential causes/mechanisms of failure

10. The probability factor “Occurrence” (O)

It is the chance that one of the specific causes will occur.

Standard scale uses 1 to represent not likely and 10 to indicate inevitable.

7. Establish a numerical ranking for the Severity(S) of the effect S is the assessment of the seriousness of the failure effect

standard scale uses 1 for no effect and 10 for very serious effect.

Used to classify any special product characteristics for components that may require additional process controls.

9. Identify the potential causes/mechanisms of failure 10. The probability factor “Occurrence” (O)

It is the chance that one of the specific causes will occur.

Standard scale uses 1 to represent not likely and 10 to indicate inevitable.

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FMEA PROCEDURE

11. Identify current controls (design or process)

12. Determine the likelihood of detection (D)

It is the assessment of the likelihood that the current controls will detect the cause of failure mode

1 used for certain of detection and 10 for uncertainty of detection.

13. Review Risk Priority Number (RPN)

RPN = S x O x D

14. Determine recommended actions

15. Assign responsibility and target completion date

16. Indicate action taken

After action, re-assess the severity, occurrence and detection and revise the RPN

17. Update the FMEA

11. Identify current controls (design or process) 12. Determine the likelihood of detection (D)

It is the assessment of the likelihood that the current controls will detect the cause 1 used for certain of detection and 10 for uncertainty of detection.

15. Assign responsibility and target completion date

assess the severity, occurrence and detection and revise the RPN

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THANK YOU

THANK

YOU

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