Introduction
The FME(C)A is a design tool used to systematically analyze postulated component failures and identify the resultant effects on system operations. The analysis is sometimes characterized as consisting of two sub-analyses, the first being the failure modes and effects analysis (FMEA), and the second, the criticality analysis (CA). Successful development of an FMEA requires that the analyst include all significant failure modes for each contributing element or part in the system. FMEAs can be performed at the system, subsystem, assembly, subassembly or part level. The FMECA should be a living document during development of a hardware design. It should be scheduled and completed concurrently with the design. If completed in a timely manner, the FMECA can help guide design decisions. The usefulness of the FMECA as a design tool and in the decision-making process is dependent on the effectiveness and timeliness with which design problems are identified. Timeliness is probably the most important consideration. In the extreme case, the FMECA would be of little value to the design decision process if the analysis is performed after the hardware is built. While the FMECA identifies all part failure modes, its primary benefit is the early identification of all critical and catastrophic subsystem or system failure modes so they can be eliminated or minimized through design modification at the earliest point in the development effort; therefore, the FMECA should be performed at the system level as soon as preliminary design information is available and extended to the lower levels as the detail design progresses. Remark: For more complete scenario modelling another type of reliability analysis may be considered, for exampleFunctional failure mode and effects analysis
The analysis should always be started by listing the functions that the design needs to fulfill. Functions are the starting point of a well done FMEA, and using functions as baseline provides the best yield of an FMEA. After all, a design is only one possible solution to perform functions that need to be fulfilled. This way an FMEA can be done on concept designs as well as detail designs, on hardware as well as software, and no matter how complex the design. When performing an FMECA, interfacing hardware (or software) is first considered to be operating within specification. After that it can be extended by consequently using one of the 5 possible failure modes of one function of the interfacing hardware as a cause of failure for the design element under review. This gives the opportunity to make the design robust for function failure elsewhere in the system. In addition, each part failure postulated is considered to be the only failure in the system (i.e., it is a single failure analysis). In addition to the FMEAs done on systems to evaluate the impact lower level failures have on system operation, several other FMEAs are done. Special attention is paid to interfaces between systems and in fact at all functional interfaces. The purpose of these FMEAs is to assure that irreversible physical and/or functional damage is not propagated across the interface as a result of failures in one of the interfacing units. These analyses are done to the piece part level for the circuits that directly interface with the other units. The FMEA can be accomplished without a CA, but a CA requires that the FMEA has previously identified system level critical failures. When both steps are done, the total process is called an FMECA.Ground rules
The ground rules of each FMEA include a set of project selected procedures; the assumptions on which the analysis is based; the hardware that has been included and excluded from the analysis and the rationale for the exclusions. The ground rules also describe the indenture level of the analysis (i.e. the level in the hierarchy of the part to the sub-system, sub-system to the system, etc.), the basic hardware status, and the criteria for system and mission success. Every effort should be made to define all ground rules before the FMEA begins; however, the ground rules may be expanded and clarified as the analysis proceeds. A typical set of ground rules (assumptions) follows: # Only one failure mode exists at a time. # All inputs (including software commands) to the item being analyzed are present and at nominal values. # All consumables are present in sufficient quantities. # Nominal power is availableBenefits
Major benefits derived from a properly implemented FMECA effort are as follows: # It provides a documented method for selecting a design with a high probability of successful operation and safety. # A documented uniform method of assessing potential failure mechanisms, failure modes and their impact on system operation, resulting in a list of failure modes ranked according to the seriousness of their system impact and likelihood of occurrence. # Early identification of single failure points (SFPS) and system interface problems, which may be critical to mission success and/or safety. They also provide a method of verifying that switching between redundant elements is not jeopardized by postulated single failures. # An effective method for evaluating the effect of proposed changes to the design and/or operational procedures on mission success and safety. # A basis for in-flight troubleshooting procedures and for locating performance monitoring and fault-detection devices. # Criteria for early planning of tests. From the above list, early identifications of SFPS, input to the troubleshooting procedure and locating of performance monitoring / fault detection devices are probably the most important benefits of the FMECA. In addition, the FMECA procedures are straightforward and allow orderly evaluation of the design.History
Procedures for conducting FMECA were described in US Armed Forces Military Procedures document MIL-P-1629 (1949); revised in 1980 as MIL-STD-1629A. By the early 1960s, contractors for the U.S. National Aeronautics and Space Administration (NASA) were using variations of FMECA or FMEA under a variety of names. NASA programs using FMEA variants includedBasic terms
The following covers some basic FMEA terminology. ;Action priority (AP) :The AP replaces the former risk matrix and RPN in the AIAG / VDA FMEA handbook 2019. It makes a statement about the need for additional improvement measures. ;Failure :The loss of a function under stated conditions. ;Failure mode :The specific manner or way by which a failure occurs in terms of failure of the part, component, function, equipment, subsystem, or system under investigation. Depending on the type of FMEA performed, failure mode may be described at various levels of detail. A piece part FMEA will focus on detailed part or component failure modes (such as fully fractured axle or deformed axle, or electrical contact stuck open, stuck short, or intermittent). A functional FMEA will focus on functional failure modes. These may be general (such as no function, over function, under function, intermittent function, or unintended function) or more detailed and specific to the equipment being analyzed. A PFMEA will focus on process failure modes (such as inserting the wrong drill bit). ;Failure cause and/or mechanism :Defects in requirements, design, process, quality control, handling or part application, which are the underlying cause or sequence of causes that initiate a process (mechanism) that leads to a failure mode over a certain time. A failure mode may have more causes. ''For example; "fatigue or corrosion of a structural beam" or "fretting corrosion in an electrical contact" is a failure mechanism and in itself (likely) not a failure mode. The related failure mode (end state) is a "full fracture of structural beam" or "an open electrical contact". The initial cause might have been "Improper application of corrosion protection layer (paint)" and /or "(abnormal) vibration input from another (possibly failed) system". ;Failure effect :Immediate consequences of a failure on operation, or more generally on the needs for the customer / user that should be fulfilled by the function but now is not, or not fully, fulfilled. ;Indenture levels (bill of material or functional breakdown) :An identifier for system level and thereby item complexity. Complexity increases as levels are closer to one. ;Local effect :The failure effect as it applies to the item under analysis. ;Next higher level effect :The failure effect as it applies at the next higher indenture level. ;End effect :The failure effect at the highest indenture level or total system. ;Detection :The means of detection of the failure mode by maintainer, operator or built in detection system, including estimated dormancy period (if applicable). ;Probability :The likelihood of the failure occurring. ;Risk priority number (RPN) :Severity (of the event) × probability (of the event occurring) × detection (probability that the event would not be detected before the user was aware of it). ;Severity :The consequences of a failure mode. Severity considers the worst potential consequence of a failure, determined by the degree of injury, property damage, system damage and/or time lost to repair the failure. ;Remarks / mitigation / actions :Additional info, including the proposed mitigation or actions used to lower a risk or justify a risk level or scenario.Example of FMEA worksheet
Probability (P)
It is necessary to look at the cause of a failure mode and the likelihood of occurrence. This can be done by analysis, calculations / FEM, looking at similar items or processes and the failure modes that have been documented for them in the past. A failure cause is looked upon as a design weakness. All the potential causes for a failure mode should be identified and documented. This should be in technical terms. Examples of causes are: Human errors in handling, Manufacturing induced faults, Fatigue, Creep, Abrasive wear, erroneous algorithms, excessive voltage or improper operating conditions or use (depending on the used ground rules). A failure mode may given a ''Probability Ranking'' with a defined number of levels. For a piece part FMEA, quantitative probability may be calculated from the results of a reliability prediction analysis and the failure mode ratios from a failure mode distribution catalog, such as RAC FMD-97. This method allows a quantitative FTA to use the FMEA results to verify that undesired events meet acceptable levels of risk.Severity (S)
Determine the Severity for the worst-case scenario adverse end effect (state). It is convenient to write these effects down in terms of what the user might see or experience in terms of functional failures. Examples of these end effects are: full loss of function x, degraded performance, functions in reversed mode, too late functioning, erratic functioning, etc. Each end effect is given a Severity number (S) from, say, I (no effect) to V (catastrophic), based on cost and/or loss of life or quality of life. These numbers prioritize the failure modes (together with probability and detectability). Below a typical classification is given. Other classifications are possible. See alsoDetection (D)
The means or method by which a failure is detected, isolated by operator and/or maintainer and the time it may take. This is important for maintainability control (availability of the system) and it is especially important for multiple failure scenarios. This may involve dormant failure ''modes'' (e.g. No direct system effect, while a redundant system / item automatically takes over or when the failure only is problematic during specific mission or system states) or latent failures (e.g. deterioration failure ''mechanisms'', like a metal growing crack, but not a critical length). It should be made clear how the failure mode or cause can be discovered by an operator under normal system operation or if it can be discovered by the maintenance crew by some diagnostic action or automatic built in system test. A dormancy and/or latency period may be entered.Dormancy or latency period
The average time that a failure mode may be undetected may be entered if known. For example: * Seconds, auto detected by maintenance computer * 8 hours, detected by turn-around inspection * 2 months, detected by scheduled maintenance block X * 2 years, detected by overhaul task xIndication
If the undetected failure allows the system to remain in a ''safe'' / working state, a second failure situation should be explored to determine whether or not an indication will be evident to all ''operators'' and what corrective action they may or should take. Indications to the operator should be described as follows: * Normal. An indication that is evident to an operator when the system or equipment is operating normally. * Abnormal. An indication that is evident to an operator when the system has malfunctioned or failed. * Incorrect. An erroneous indication to an operator due to the malfunction or failure of an indicator (i.e., instruments, sensing devices, visual or audible warning devices, etc.). PERFORM DETECTION COVERAGE ANALYSIS FOR TEST PROCESSES AND MONITORING (From ARP4761 Standard): This type of analysis is useful to determine how effective various test processes are at the detection of latent and dormant faults. The method used to accomplish this involves an examination of the applicable failure modes to determine whether or not their effects are detected, and to determine the percentage of failure rate applicable to the failure modes which are detected. The possibility that the detection means may itself fail latently should be accounted for in the coverage analysis as a limiting factor (i.e., coverage cannot be more reliable than the detection means availability). Inclusion of the detection coverage in the FMEA can lead to each individual failure that would have been one effect category now being a separate effect category due to the detection coverage possibilities. Another way to include detection coverage is for the FTA to conservatively assume that no holes in coverage due to latent failure in the detection method affect detection of all failures assigned to the failure effect category of concern. The FMEA can be revised if necessary for those cases where this conservative assumption does not allow the top event probability requirements to be met. After these three basic steps the Risk level may be provided.Risk level (P×S) and (D)
Risk is the combination of end effect probability and severity where probability and severity includes the effect on non-detectability (dormancy time). This may influence the end effect probability of failure or the worst case effect Severity. The exact calculation may not be easy in all cases, such as those where multiple scenarios (with multiple events) are possible and detectability / dormancy plays a crucial role (as for redundant systems). In that case fault tree analysis and/or event trees may be needed to determine exact probability and risk levels. Preliminary risk levels can be selected based on aTiming
The FMEA should be updated whenever: * A new cycle begins (new product/process) * Changes are made to the operating conditions * A change is made in the design * New regulations are instituted * Customer feedback indicates a problemUses
* Development of system requirements that minimize the likelihood of failures. * Development of designs and test systems to ensure that the failures have been eliminated or the risk is reduced to acceptable level. * Development and evaluation of diagnostic systems. * To help with design choices (trade-off analysis).Advantages
* Catalyst for teamwork and idea exchange between functions * Collect information to reduce future failures, capture engineering knowledge * Early identification and elimination of potential failure modes * Emphasize problem prevention * Fulfill legal requirements (product liability) * Improve company image and competitiveness * Improve production yield * Improve the quality, reliability, and safety of a product/process * Increase user satisfaction * Maximize profit * Minimize late changes and associated cost * Reduce impact on company profit margin * Reduce system development time and cost * Reduce the possibility of same kind of failure in future * Reduce the potential for warranty concernsLimitations
While FMEA identifies important hazards in a system, its results may not be comprehensive and the approach has limitations. In the healthcare context, FMEA and other risk assessment methods, including SWIFT ( Structured What If Technique) and retrospective approaches, have been found to have limited validity when used in isolation. Challenges around scoping and organisational boundaries appear to be a major factor in this lack of validity. If used as aTypes
* Functional: before design solutions are provided (or only on high level) functions can be evaluated on potential functional failure effects. General Mitigations ("design to" requirements) can be proposed to limit consequence of functional failures or limit the probability of occurrence in this early development. It is based on a functional breakdown of a system. This type may also be used for Software evaluation. * Concept design / hardware: analysis of systems or subsystems in the early design concept stages to analyse the failure mechanisms and lower level functional failures, specially to different concept solutions in more detail. It may be used in trade-off studies. * Detailed design / hardware: analysis of products prior to production. These are the most detailed (in MIL 1629 called Piece-Part or Hardware FMEA) FMEAs and used to identify any possible hardware (or other) failure mode up to the lowest part level. It should be based on hardware breakdown (e.g. the BoM = bill of materials). Any failure effect severity, failure prevention (mitigation), failure detection and diagnostics may be fully analyzed in this FMEA. * Process: analysis of manufacturing and assembly processes. Both quality and reliability may be affected from process faults. The input for this FMEA is amongst others a work process / task breakdown.See also
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