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Introduction to FMEA

5
  • What is Risk in FMEA? Why Prevention Important?
  • Introduction to FMEA | Purpose & Key Benefits
  • History of FMEA – NASA to AIAG to AIAG-VDA
  • Types of FMEA – DFMEA, PFMEA, and FMEA-MSR
  • FMEA in APQP & IATF 16949 Context

Foundations of FMEA

7
  • Function Requirement Failure in FMEA
  • Severity in FMEA (AIAG-VDA) | Explained with Examples
  • Occurrence in FMEA (AIAG-VDA) | Explained with Examples
  • Detection in FMEA (AIAG-VDA) | Explained with Examples
  • RPN vs Action Priority (AP) – Why RPN is Outdated
  • FMEA Linkages – ISO 9001, IATF 16949, APQP, PPAP.
  • Why AIAG-VDA 7-Step Approach?

Step-1: Planning & Preparation in FMEA

4
  • Step 1 – Planning & Preparation in FMEA (AIAG-VDA Standard)
  • The Five Ts in FMEA – Intent, Timing, Team, Task, Tools
  • Defining Scope, Boundaries & Assumptions in FMEA
  • Cross-Functional Team Formation in FMEA

Step 2: Structure Analysis in FMEA

4
  • Step 2 – Structure Analysis in FMEA
  • System, Subsystem, and Component Breakdown in FMEA
  • Process Flow – Structure Tree & Block Diagram in FMEA
  • Motor Stator Winding – Structure Analysis in FMEA Example

Step 3: Function Analysis in FMEA

3
  • Step 3 – Function Analysis in FMEA
  • Defining Functions & Requirements in FMEA
  • How to Write Measurable Requirements in FMEA

Step 4: Failure Analysis in FMEA

6
  • Step 4 – Failure Analysis in FMEA (Failure Modes, Effects, Causes)
  • Function Net in FMEA | Chain of Functions
  • Failure at Mode Level – Failure Modes
  • Effects of Failure in FMEA
  • Causes of Failure in FMEA (Design vs Process)
  • Cascading Failures – Failure Cause Mode Effect Relationship in FMEA

Step 5: Risk Analysis in FMEA

9
  • Current Detection Controls in FMEA
  • Current Prevention Controls in FMEA (AIAG-VDA Standard)
  • Risk Evaluation in FMEA
  • Action Priority (AP) vs RPN in FMEA
  • Action Priority in FMEA (AIAG-VDA Standard)
  • Step 5 – Risk Analysis in FMEA
  • Severity in FMEA (AIAG-VDA) | Explained with Examples
  • Occurrence in FMEA (AIAG-VDA) | Explained with Examples
  • Detection in FMEA (AIAG-VDA) | Explained with Examples

Step 6: Optimization in FMEA

2
  • Tracking & Closing Actions in FMEA
  • Step 6 – Optimization in FMEA

Step 7: Results Documentation in FMEA

3
  • Customer Communication & Lessons Learned in FMEA
  • FMEA Report (Summary Table)
  • Step 7 – Results Documentation in FMEA

DFMEA in Practice

8
  • DFMEA in Practice – Step‑by‑Step
  • DFMEA Audit Readiness
  • DFMEA Optimization Step
  • DFMEA Risk Analysis
  • DFMEA Failure Analysis
  • DFMEA Function Analysis
  • DFMEA Structure Analysis
  • Product Snapshot – DFMEA in Practice (Step-by-Step)

PFMEA in Practice

10
  • PFMEA Audit Readiness
  • PFMEA Results Documentation
  • PFMEA Optimization step
  • PFMEA Risk Analysis
  • PFMEA Failure Analysis
  • PFMEA Function Analysis
  • PFMEA Structure Analysis
  • PFMEA Planning and Preparation
  • PFMEA Process Snapshot
  • PFMEA in Practice – Step‑by‑Step

FMEA Linkages

5
  • 📘 Case Study: How DFMEA Links to PFMEA and Control Plan — A Practical Guide
  • How FMEA Links to PPAP Deliverables
  • Prevention and Detection Controls in PFMEA to Control Plan | How to Link Them
  • How FMEA Drives Control Plans in Manufacturing Quality
  • FMEA and Control Plan Linkage

FMEA Tools & Templates

3
  • Excel vs Professional FMEA Software: Explain
  • FMEA in APIS IQ, PLATO SCIO, and Knowlence TDC: Overview of Top FMEA Software Tools
  • Excel-Based AIAG-VDA FMEA Template (Walkthrough)

FMEA Best Practices

2
  • FMEA Moderation: Common Mistakes & Best Practices
  • Common Mistakes & Best Practices in FMEA Creation

FMEA Advanced Applications

12
  • Future of FMEA – AI, Automation & Digital Technology
  • FMEA Use Cases in EVs, Welding, Electronics & Embedded Systems
  • Internal & Customer FMEA Audit Preparation
  • FMEA Moderation Techniques for Cross-Functional Teams
  • Advanced Failure Cause Modeling in FMEA
  • Family FMEA – Save Time Across Product Lines
  • FMEA in APQP Phases and Project Milestones
  • Using FMEA in Functional Safety (ISO 26262)
  • What is System FMEA? Scope, Structure & Interface Analysis
  • Which FMEA Software Should You Choose?
  • Software for FMEA
  • How FMEA Links with Control Plan, PPAP & Special Characteristics
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  • PFMEA Failure Analysis

PFMEA Failure Analysis

FMEA Expert
Updated on September 6, 2025

7 min read

🧭 Why Step 4? #

You defined what each station must achieve in Step 3. Now ask:

“How can each function fail, why would it fail, and what happens if it does?”

This step creates the backbone of your risk evaluation: unambiguous chains that will be rated in Step 5 and improved in Step 6.


🎯 Objectives #

  • Write precise, testable Failure Modes (deviations from Step-3 specs).
  • Trace Effects at the next operation/line and the end user/vehicle.
  • Identify specific Causes using 6M (Man, Machine, Method, Material, Measurement, Mother Nature).
  • List current Prevention & Detection controls (as-is), and set initial Severity (S).

🧩 What “good” looks like #

  • Function: Press impeller to 12.00 ± 0.05 mm with OK force-distance signature
  • Failure Mode (FM): Press depth undersize (<11.95 mm) or oversize (>12.05 mm); signature out-of-window
  • Effect (Line): Low retention → slip at run-up / early leak
  • Effect (End User): Low/zero flow → engine overheat; leak complaint
  • Cause: Fixture hard-stop drift; excessive lube; shaft OD low; press profile mis-set
  • Prevention: Hard-stop setting SOP + PM; incoming OD control; lube spec
  • Detection: LVDT 100% + signature window; SPC depth chart; daily master checks
  • S (initial): 10 (engine overheat if undetected & shipped)

Rule of thumb: Write FMs as measurable deviations; write Effects at two levels (line + end user); write Causes at component/tool/method granularity.


🔗 Severity Anchors (examples) #

  • S=10: Safety or regulation-critical user effect (e.g., engine overheat due to insufficient flow).
  • S=8–9: Major vehicle function loss (e.g., coolant leak leading to breakdown).
  • S=6–7: Performance degradation/latent field failure (e.g., intermittent electrical).
  • S=4–5: Nuisance/customer dissatisfaction (noise, rework only).
    (Confirm exact scale per your AIAG-VDA table/customer CSRs.)

📋 PFMEA Failure Chains — Worked Examples (copy into your sheet) #

#Station (Op)Function (from Step 3)Failure Mode (deviation)Effect – Next Process/LineEffect – End User/VehicleSLikely Causes (6M)Current Prevention ControlsCurrent Detection ControlsEvidence/Notes
1OP05 Press-fitPress impeller to 12.00 ± 0.05 mm; signature OKDepth undersize/oversize; signature out-of-windowLow retention, slip at OP11 spinLow/zero flow → overheat10Machine: hard-stop drift; Method: wrong press profile; Material: shaft OD low; Man: lube over-applyHard-stop setup SOP; profile locked; incoming OD spec; lube specLVDT 100%, force signature match; SPC; daily masterKeep last 30 subgroup chart; master results
2OP05 Press-fitsameSpline/impeller crack (overforce)Crack propagates; early failureLeak/low flow field failure8Machine: press over-force; Material: brittle impeller lot; Method: no soft-startForce window limits; supplier COASignature window; visual auditCOA + incident log
3OP06 Seal installInstall seal orientation; cleanlinessSeal mis-orientation / damaged lipFail at OP10/12; reworkCoolant leak at customer8Man: handling; Machine: nest mis-align; Environment: cleanlinessGuided fixture; chamfers; handling WIVision 100%; particle gate; OP10 pre-leakVision false accept rate trending
4OP06 Seal installMaintain shaft Ra ≤0.30 µmSurface roughness highAccelerated wearLeak in service8Material: incoming shaft finish; Method: skipped auditCOA; Ra audit planOP10/12 tests (late); random Ra measurementConsider earlier Ra check
5OP07 Potting/ESDDispense mass/time; cure profile; ESD <100 VESD event uncontrolled (no strap/mat fail)Latent PCB damage; passes OP11Intermittent failure in field9Measurement: ESD tester faulty; Method: bypass checks; Environment: dry airESD policy; start-of-shift checkESD monitor log (manual); OP11 may not detectD likely high; plan continuous monitor
6OP07 PottingMass/time; cure profileMass low / voids; under-cureMoisture ingress; OP11 pass; OP12 passEarly electronics failure7Machine: dispenser drift; Method: wrong recipe; Material: resin agedRecipe lock; PM on dispenser; FEFO for resinScale log 100%; cure profile logAdd in-process mass check
7OP09 TorqueTighten to 4.0 ± 0.3 N·m + angleUnder-torqueJoint loosening; leak at OP12Leak / vibration in field9Machine: tool calibration drift; Method: wrong strategy; Man: wrong socketTorque strategy; tool cal schedule100% torque/angle trace; socket IDDaily audit curves
8OP09 TorquesameOver-torque / cross-threadCracked housing; scrap/reworkLeak in service8Man: mis-start; Machine: tool strategy; Material: thread burrsThread-start aid; SOPCurve pattern check; visual thread checkAdd thread forming guidance
9OP10 Pre-leakAir decay ≤ X @ 1.0 barBench recipe mis-set / leak at fixtureFalse pass/false fail; late discovery at OP12Leak reaches customer if OP12 bypassed8Method: unlocked recipe; Machine: valve seal wearRecipe lock; PM sealsDaily master part; result to MESIf both weak → high D
10OP12 Final leak/flowLeak ≤0.5 @1.5 bar; Flow ≥35 L/min @ ΔP 20 kPaRecipe wrong / test bypassUnit ships untestedLeak / overheat in field10Measurement: role mis-config; Tool: bench comms lost; Method: manual overrideMES role-based lock; No scan → no progress gateAuto-upload curves; bench heartbeatAudit logs reviewed?
11OP12 Final flowFlow ≥35 L/min @ ΔP 20 kPaMeter mis-cal / clogged filter → false passLow flow escapesOverheat in field10Measurement: missed cal; Environment: temp/viscosityCal matrix; temp comp; filter PMDaily master at 2 points; curve plausibilityAdd dual-check (ΔP vs RPM sanity)
12OP01 KittingAssign serial; verify kitWrong impeller variant in kitFail at OP12 (low flow)Overheat in field if undetected10Material: barcode duplication; Man: kit mix; Method: no double-scanTwo-scan check; kit layout; color codingScanner + MES kit check 100%Add vision shape check
13Interface – MESNo scan → no progressGate disabled / role overrideDownstream tests not tied to unitUntested unit ships10Method: IT role; Machine: network outageRole policy; IT change controlGate audit logAdd automated alerts
14OP08 ConnectorFit/Join per specMis-seat / incomplete crimpIntermittent current; OP11 fail or passIntermittent field failure7Man: technique; Machine: crimp wear; Measurement: pull test gapCrimp PM; WI with photosPull test (sample); vision 100% for featuresIncrease sample on pull

How to use: Keep Functions identical to Step 3 wording. Phrase FMs as quantified deviations. List Effects at both levels. Causes should be specific and verifiable. Controls reflect current state only (don’t pre-write actions).


🧠 Writing Tips (with examples) #

Bad FM: “Press not OK.”
Good FM: “Press depth <11.95 mm or >12.05 mm OR force signature outside window.”

Bad Cause: “Operator error.”
Good Cause: “Operator applied excess lube (2× spec) causing hydraulic lock,” or “Hard-stop set +0.15 mm post-PM.”

Effects: Always include line effect (scrap/rework/late detection) and end-user effect (safety, regulatory, performance). Severity is set from the end-user effect if the defect escapes.


🧯 Prevention vs Detection (don’t mix them) #

  • Prevention controls influence Occurrence (O) (design of process: fixtures, recipes, tooling strategy, PM, training, incoming controls).
  • Detection controls influence Detection (D) (what checks/tests can catch the defect before ship: gages, benches, vision, SPC, interlocks, curve storage).

In Step 5, justify O with evidence (capability, PM compliance, MSA). Justify D with coverage & timing (100% vs sampled, early vs late, automated vs manual).


🧱 6M Cause Library (starter list to seed brainstorming) #

  • Man: certification lapsed; fatigue; ESD strap not worn; wrong socket; improper lube technique.
  • Machine: servo press drift; DC tool calibration; vision lighting; leak bench valve leak; flow meter drift.
  • Method: recipe unlocked; wrong press profile; missing thread-start step; potting start/stop timing; no “no scan → no progress.”
  • Material: impeller ID spread; brittle batch; seal hardness out of spec; resin past shelf life; wrong screw finish.
  • Measurement: LVDT out of cal; master part unstable; pull tester mis-zero; temp probe offset.
  • Mother Nature: humidity <30% (ESD risk); temp shift affecting viscosity and ΔP; airborne particles at seal station.

📑 Template (paste into your PFMEA workbook) #

Process StepFunction (from Step 3)Failure Mode (deviation)Effect – LineEffect – End UserSCause (6M)Current PreventionCurrent DetectionNotes/Evidence

(Fill one row per failure chain. Add your PFMEA Row ID to link later to Control Plan and Actions.)


✅ Outputs of Step 4 #

  • ✅ Clear Cause → Failure Mode → Effects chains for each critical station & interface.
  • ✅ Initial Severity (S) assigned from the end-user effect.
  • ✅ Current controls captured, ready to justify O and D in Step 5.
  • ✅ A prioritized list of chains to rate first (press-fit, seal, torque, leak/flow, ESD, MES gates).

⚠️ Common Pitfalls (and fixes) #

PitfallFix
Vague FMs (“not ok”)Use measurable deviations & thresholds.
Effects only at line levelAdd end-user effect; S comes from there.
Generic causes (“operator error”)Make causes specific and auditable.
Controls written as future actionsDocument current controls only; actions are Step 6.
Skipping interfaces (MES, recipe lock)Add interface rows—they prevent major escapes.

🔗 What’s Next #

Proceed to Lesson 5.5 — Step 5: Risk Analysis (S-O-D & AP). You’ll assign Occurrence and Detection ratings using the controls listed here and determine Action Priority (AP) to drive Step 6 improvements.


🧠 Pro Tip #

If you can’t point to evidence (MSA, calibration, SPC, PM logs, master checks) for a control, assume D will be weaker (higher) and O higher—and plan to fix it in Step 6.

Updated on September 6, 2025

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PFMEA Risk AnalysisPFMEA Function Analysis
Table of Contents
  • 🧭 Why Step 4?
  • 🎯 Objectives
  • 🧩 What “good” looks like
  • 🔗 Severity Anchors (examples)
  • 📋 PFMEA Failure Chains — Worked Examples (copy into your sheet)
  • 🧠 Writing Tips (with examples)
  • 🧯 Prevention vs Detection (don’t mix them)
  • 🧱 6M Cause Library (starter list to seed brainstorming)
  • 📑 Template (paste into your PFMEA workbook)
  • ✅ Outputs of Step 4
  • ⚠️ Common Pitfalls (and fixes)
  • 🔗 What’s Next
  • 🧠 Pro Tip
  • Free FMEA Course
  • Services
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