View Categories

D5 step – Choose Corrective Action in 8D

2 min read

What Is choose corrective action step in 8D Process? #

Once the root causes are identified and verified in step D4, the next step is D5: Choose Corrective Action. It is focuses on selecting permanent, verified actions that eliminate root causes.

At this stage, containment action (D3) is still active, but now we’re designing long-term solutions that prevent repeated failure and make sure a stable product quality.

“Containment protects the customer; corrective action protects the future.”

Therefore, the Objective of choose corrective action is to:

  • Define permanent corrective actions (PCAs) that directly act on verified root causes.
  • Ensure each corrective action is specific, measurable, and verifiable.
  • Identify responsibility and target dates for each action.
  • Check action feasibility before implementation (technical, resource, and timing checks).
  • Plan evidence for verification (process data, trials, inspection results).

How to choose corrective actions (Explained) #

Let’s understand in our 8D report using same example.

From our previous step:

TypeVerified Root Cause
Occurrence root CauseGas regulator O-ring worn out → unstable gas flow → weak weld.
Non-Detection root CausePoor lighting in inspection area → weak joints passed undetected.

Both need targeted corrective actions, to avoid repeated customer complaint.


Brainstorm Corrective Actions

Plan a cross-functional team discussion (CFT) to list all feasible long-term actions that eliminate or prevent the verified root causes.

For Example

Cause TypeRoot CausePossible Corrective Actions
OccurrenceGas regulator O-ring worn1. Replace worn regulator.
2. Include regulator inspection in PM schedule.
3. Change supplier to better O-ring material.
4. Add flowmeter with low-pressure alarm.
Non-DetectionPoor lighting at inspection station1. Replace damaged lamp immediately.
2. Implement preventive maintenance checklist for lighting.
3. Introduce Lux-level standard for QA areas.
4. Conduct operator retraining on weld-defect identification.

Next, evaluate which actions are practical, sustainable, and measurable.


Fill the “Corrective Action” in Template

Root Cause TypeCorrective Action Planned / TakenTarget DateCompletion DateResponsibility
OccurrenceReplace faulty gas regulator; update Preventive Maintenance (PM) checklist to include regulator O-ring inspection every 3 months; add inline gas-flow indicator.18 Oct 202520 Oct 2025Maintenance Engineer – Kiran Deshmukh
Non-DetectionReplace non-functional inspection lamp; install two LED lights (min. 800 Lux); create PM checklist for lighting; retrain inspectors on weld visual criteria.18 Oct 202521 Oct 2025QA Engineer – Rahul Patil

Filled D5 Section (From Template)

FieldExample Entry
Root Cause (Occurrence)Gas regulator O-ring worn → unstable gas flow.
Corrective ActionReplace all regulators with new design; include O-ring check in PM checklist; install flow indicator.
Root Cause (Non-Detection)Poor lighting at inspection station.
Corrective ActionReplace inspection lamps; establish PM checklist; verify Lux level weekly; retrain inspectors.
ResponsibilityMaintenance Engineer (Kiran D.) & QA Engineer (Rahul P.)
Target Date20 Oct 2025
Completion Date21 Oct 2025
Approved ByQuality Manager – Rajesh Kulkarni

Evidence Collection for next step (D6) Verification

Prepare objective proof that your corrective actions were implemented as planned:

  • Photographs of new regulators and lighting setup.
  • Updated PM checklists (signed by maintenance).
  • Training attendance sheets for QA inspectors.
  • Trial weld results and inspection data.

These documents will be attached in the D6 – Implement & Validate stage.


Common Mistakes to Avoid in D5 step #

  1. Choosing quick fixes instead of systemic actions.
    e.g., “tightened regulator” instead of replacing or adding PM system.
  2. No data-based validation.
    Implementing action without proof of effectiveness.
  3. Ignoring cost or feasibility.
    Plan must be practical and sustainable.
  4. Skipping approval process.
    Always document Champion and customer approvals.
  5. No linkage to FMEA or Control Plan.
    Preventive control must appear in updated documentation (D7).

How D5 Links to next steps

Once you choose corrective action, the next steps are to verify and validate it:

  1. D6 – Implement and Validate Corrective action = Selected actions must now be implemented and validated in real conditions.
  2. D7 – Prevent Recurrence = Proven actions get standardized into control documents.

Summary of step D5 #

  • D5 focuses on permanent corrective actions, not temporary containment.
  • Each action must directly eliminate a verified root cause.
  • Validate feasibility, assign responsibility, and document timelines.
  • Collect evidence for verification in D6.
  • Always align with FMEA and Control Plan for future prevention.

“If the cause is verified, but the action is weak, the problem will occure back soon.”

Scroll to Top