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FMEA is a method for analyzing potential reliability problems, early in the development cycle. It is used to identify potential failure modes, determine their effect on the operation of the product, and identify actions to mitigate the failures. A crucial step is anticipating what might go wrong with a product.
FMEA is a method for analyzing potential reliability problems, early in the development cycle. It is used to identify potential failure modes, determine their effect on the operation of the product, and identify actions to mitigate the failures. A crucial step is anticipating what might go wrong with a product.
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FMEA is a method for analyzing potential reliability problems, early in the development cycle. It is used to identify potential failure modes, determine their effect on the operation of the product, and identify actions to mitigate the failures. A crucial step is anticipating what might go wrong with a product.
Copyright:
Attribution Non-Commercial (BY-NC)
Verfügbare Formate
Als PPT, PDF, TXT herunterladen oder online auf Scribd lesen
(FMEA) ntroduction: t is a method for analyzing potential potential reliability problems, early in the development cycle, where it is easier to take actions to overcome these issues, thereby enhancing reliability through design. FMEA is used to identify potential failure modes, determine their effect on the operation of the product, and identify actions to mitigate the failures. A crucial step is anticipating what might go wrong with a product. While anticipating every failure mode is not possible, the development team should formulate as extensive a list of potential failure modes as possible. 2 %ypes of FMEA: System FMEA focuses on global system functions Design FMEA (DFMEA) focuses on components and subsystems !74.ess FMEA focuses on manufacturing and assembly processes Se7;i.e FMEA focuses on service functions S41twa7e FMEA focuses on software functions 3 esign Failure Mode Effects Analysis (FMEA) t is an application of FMEA method specifically for product design t is a method used in engineering to document and explore ways that a product design might fail in realworld use 4 !rimary Objective %he primary objective of a FMEA is to uncover potential failures associated with the product that could cause: !roduct malfunctions. Shortened product life. Safety hazards while using the product. FMEAs should be used throughout the design process from !reliminary design until the product goes into production. 5 %ypes of DFMEA %here are three types of FMEA System FMEA Sub System FMEA Component FMEA 6 System DFMEA %he FMEA will always take the feed from the Boundary and ! (!arameter) diagram. %he ideal output from the boundary diagram will become the desired or required function in the FMEA. n the case of System FMEA, the cause will always be the inability to receive the ideal input/interface function of the surrounding sub system. 7 Sub System DFMEA %here is little difference between the system FMEA and Sub System FMEA. n the Sub system FMEA the cause of failures are component. Consider the same %ransmission as a system and !lanetary system as a sub system, which as piston, gears etc as components. n this case, look up the boundary diagram, to get to ideal inputs and outputs. n case of the planetary system we have, function as providing adequate gear ratio. %he failure mode associated with this are as following nadequate gear ratio ntermittent gear ratio No gear ratio 8 Component FMEA n the Component FMEA the cause of failures are specific design features or geometry. 9 Steps to Conduct a DFMEA Step 1 Re;iew the designUse a blueprint or schematic of the design/product Step 2 B7ainst47m p4tentiaI 1aiIu7e m4desReview existing documentation Step 3 List p4tentiaI e11e.ts 41 1aiIu7e%here may be more than one for each Step 4 Assign Se;e7ity 7ankingsBased on the severity of the consequences of Step 5 lAssign O..u77en.e 7ankingsBased on how frequently the cause of the failure is likely to occur. CONTINUE . . . 10 Steps to Conduct a FMEA Step 6 Assign Dete.ti4n 7ankingsBased on the chances the failure will be detected prior to the customer finding it. Step 7 CaI.uIate the R!NSeverity x Occurrence x etection. Step 8 De;eI4p the a.ti4n pIanefine who will do what by when. Step 9 Take a.ti4nmplement the improvements identified by your FMEA team. Step 10 CaI.uIate the 7esuIting R!NReevaluate each of the potential failures once improvements have been made and determine their impact on the R!Ns. 11 Step : Review the esign Reas4ns 147 the 7e;iew: elp assure all team members are familiar with the product and its design. dentify each of the main components of the design and determine the function or functions of those components and interfaces between them. Make sure you are studying all components defined in the scope of the FMEA. Use a p7int 47 s.hemati. 147 the 7e;iew. Add Reference Numbers to each component and interface. T7y 4ut a p74t4type 47 sampIe. nvite a subject matter expert to answer questions. ocument the function(s) of each component and interface. 12 Step 2: Brainstorm !otential Failure Modes C4nside7 p4tentiaI 1aiIu7e m4des 147 ea.h .4mp4nent and inte71a.e. A potential failure mode represents any manner in which the product component could fail to perform its intended function or functions. Remember that many components will have more than one failure mode. ocument each one. o not leave out a potential failure mode because it rarely happens. on't take shortcuts here; this is the time to be thorough. !7epa7e 147 the b7ainst47ming a.ti;ity. Before you begin the brainstorming session, review documentation for clues about potential failure modes. Use customer complaints, warranty reports, and reports that identify things that have gone wrong, such as hold tag reports, scrap, damage, and rework, as inputs for the brainstorming activity. Additionally, consider what may happen to the product under difficult usage conditions and how the product might fail when it interacts with other products. 13 Step 3: List !otential Effects of Failure The e11e.t is 7eIated di7e.tIy t4 the abiIity 41 that spe.i1i. .4mp4nent t4 pe7147m its intended 1un.ti4n. An effect is the impact a failure could make should it occur. Some failures will have an effect on customers; others on the environment, the process the product will be made on, and even the product itself. The e11e.t sh4uId be stated in te7ms meaning1uI t4 p74du.t pe7147man.e. I1 the e11e.ts a7e de1ined in gene7aI te7ms, it wiII be di11i.uIt t4 identi1y (and 7edu.e) t7ue p4tentiaI 7isks. 14 Step 4: Assign Severity Rankings The 7anking s.aIes a7e missi4n .7iti.aI 147 the su..ess 41 a DFMEA be.ause they estabIish the basis 147 dete7mining 7isk 41 4ne 1aiIu7e m4de and e11e.t 7eIati;e t4 an4the7. The same 7anking s.aIes 147 DFMEAs sh4uId be used .4nsistentIy th74ugh4ut an 47ganizati4n. This wiII make it p4ssibIe t4 .4mpa7e the R!Ns 174m di11e7ent FMEAs t4 4ne an4the7. %he severity ranking is based on a relative scale ranging from to . A " means the effect has a dangerously high severity leading to a hazard without warning. Conversely, a severity ranking of " means the severity is extremely low. %he scales provide a relative, not an absolute, scale. See FMEA Checklists and Forms for an example FMEA Severity Ranking Scale. CONTINUE . . . 15 Step 4: Assign Severity Rankings The best way t4 .ust4mize a 7anking s.aIe is t4 sta7t with a standa7d gene7i. s.aIe and then m4di1y it t4 be m47e meaning1uI t4 y4u7 47ganizati4n. By adding organizationspecific examples to the ranking definitions, FMEA teams will have an easier time using the scales. %he use of examples saves teams time and improves the consistency of rankings from team to team. As you add examples specific to your organization, consider adding several columns with each column focused on a topic. One topic could provide descriptions of severity levels for customer satisfaction failures and another for environmental, health, and safety issues. owever, remember that each row should reflect the same relative impact, or severity, on the organization or customer See FMEA Checklists and Forms for an example of Custom FMEA Ranking Scales. (Examples of custom scales for severity, occurrence, and detection rankings are included in this Appendix.) 16 Step 5: Assign Occurrence Rankings We need to know the potential cause to determine the occurrence ranking because, just like the severity ranking is driven by the effect, the occurrence ranking is a function of the cause. %he occurrence ranking is based on the likelihood, or frequency, that the cause (or mechanism of failure) will occur. f we know the cause, we can better identify how frequently a specific mode of failure will occur. %he occurrence ranking scale, like the severity ranking, is on a relative scale from to . An occurrence ranking of " means the failure mode occurrence is very high; it happens all of the time. Conversely, a " means the probability of occurrence is remote. See FMEA Checklists and Forms for an example FMEA Occurrence Ranking Scale. CONTINUE . . . 17 Step 5: Assign Occurrence Rankings Your organization may need to customize the occurrence ranking scale to apply to different levels or complexities of design. t is difficult to use the same scale for a modular design, a complex design, and a custom design. Some organizations develop three different occurrence ranking options (time based, eventbased, and piecebased) and select the option that applies to the design or product. See FMEA Checklists and Forms for an examples of Custom FMEA Ranking Scales (Examples of custom scales for severity, occurrence, and detection rankings are included in this Appendix.) 18 Step 6: Assign etection Rankings %o assign detection rankings, consider the design or productrelated controls already in place for each failure mode and then assign a detection ranking to each control. %hink of the detection ranking as an evaluation of the ability of the design controls to prevent or detect the mechanism of failure. !revention controls are always preferred over detection controls. !revention controls prevent the cause or mechanism of failure or the failure mode itself from occurring; they generally impact the frequency of occurrence. !revention controls come in different forms and levels of effectiveness. etection controls detect the cause, the mechanism of failure, or the failure mode itself after the failure has occurred BU% before the product is released from the design stage. A detection ranking of " means the chance of detecting a failure is almost certain. Conversely, a " means the detection of a failure or mechanism of failure is absolutely uncertain. %o provide FMEA teams with meaningful examples of esign Controls, consider adding examples tied to the etection Ranking scale for design related topics such as: esign Rules FA/FM (design for assembly and design for manufacturability) ssues Simulation and Verification %esting 19 Step 7: Calculate the R!N %he R!N is the Risk !riority Number. %he R!N gives us a relative risk ranking. %he higher the R!N, the higher the potential risk. %he R!N is calculated by multiplying the three rankings together. Multiply the Severity Ranking times the Occurrence Ranking times the etection Ranking. Calculate the R!N for each failure mode and effect. Editorial Note: %he current FMEA Manual from AAG suggests only calculating the R!N for the highest effect ranking for each failure mode. We do not agree with this suggestion; we believe that if this suggestion is followed, it will be too easy to miss the need for further improvement on a specific failure mode. Since each of the three relative ranking scales ranges from to , the R!N will always be between and . %he higher the R!N, the higher the relative risk. %he R!N gives us an excellent tool to prioritize focused improvement efforts. 20 Step 8: evelop the Action !lan %aking action means reducing the R!N. %he R!N can be reduced by lowering any of the three rankings (severity, occurrence, or detection) individually or in combination with one another. A reduction in the Severity Ranking for a FMEA is often the most difficult to attain. t usually requires a design change. Reduction in the Occurrence Ranking is accomplished by removing or controlling the potential causes or mechanisms of failure. And a reduction in the etection Ranking is accomplished by adding or improving prevention or detection controls. What is considered an acceptable R!N? %he answer to that question depends on the organization. For example, an organization may decide any R!N above a maximum target of 2 presents an unacceptable risk and must be reduced. f so, then an action plan identifying who will do what by when is needed. 21 Step 9: %ake Action %he Action !lan outlines what steps are needed to implement the solution, who will do them, and when they will be completed. A simple solution will only need a Simple Action !lan while a complex solution needs more thorough planning and documentation. Most Action !lans identified during a FMEA will be of the simple "who, what, & when category. Responsibilities and target completion dates for specific actions to be taken are identified. Sometimes, the Action !lans can trigger a fairly largescale project. f that happens, conventional project management tools such as !ER% Charts and Gantt Charts will be needed to keep the Action !lan on track. 22 Step : Recalculate the Resulting R!N %his step in a FMEA confirms the action plan had the desired results by calculating the resulting R!N. %o recalculate the R!N, reassess the severity, occurrence, and detection rankings for the failure modes after the action plan has been completed. 23 %OOLS FOR FMEA %here are many tools to aid the FMEA team in reducing the relative risk of those failure modes requiring action. %he following recaps some of the most powerful action tools for FMEAs. Design 41 Expe7iments (DOE): A family of powerful statistical improvement techniques that can identify the most critical variables in a design and the optimal settings for those variables. Mistake-!7441ing (!4ka Y4ke): %echniques that can make it impossible for a mistake to occur, reducing the Occurrence ranking to . Especially important when the Severity ranking is . Design 147 AssembIy and Design 147 Manu1a.tu7abiIity (DFA/DFM) %echniques that help simplify assembly and manufacturing by modularizing product subassemblies, reducing components, and standardizing components. SimuIati4ns: Simulation approaches include preproduction prototypes, computer models, accelerated life tests, and valueengineering analyses. 24 http://www.npdsolutions.com/fmea.html http://myapqp.com/FMEA.aspx http://www.qualitytrainingportal.com/resources/ fmea/fmea_step_dfmea.htm