Free root cause analysis template
Free root cause analysis template (PDF). 5 Whys, fishbone diagrams, contributing factors, corrective actions and verification.
Updated 28 Sept 2026
Root Cause Analysis Template
| # | Name | Position / Role | Department |
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The PDF includes all 4 numbered rows, ready to print or fill on screen.
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Short answer
A root cause analysis template records the problem, evidence, analysis method such as 5 Whys or a fishbone, the root and contributing causes, corrective actions and a check that they worked. Teams run one after significant incidents, failures or nonconformities, not on a schedule. ISO 9001:2026 clause 10.2 covers nonconformity and corrective action, and ISO 45001:2018 clause 10.2 covers incidents.
Checked against ISO 9001:2026 (Edition 6, published 16 September 2026) on by the MapTrack templates team. How we check templates
Key takeaways
- The MapTrack root cause analysis template has 3 columns and room for 4 entries. Columns: Name, Position / Role, Department.
- ISO 9001:2026 clause 10.2 covers acting on nonconformities, eliminating their causes and checking the corrective action worked.
- The model WHS Act sets no express duty to investigate; regulation 38 requires controls to be reviewed when they fail.
- Investigation timeframes such as within days or within two weeks are internal practice, not legal deadlines.
- Collect evidence before analysis, then separate the root cause from contributing factors.
- Track each corrective action to closure and verify it worked before closing the RCA.
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Used by construction, mining and field service teams
What is a root cause analysis template?
A root cause analysis (RCA) template is a structured document used to systematically investigate an incident, failure, non-conformance or undesirable outcome to identify its underlying cause rather than just its symptoms. It guides investigators through defining the problem, collecting evidence, analysing contributing factors using structured methodologies (5 Whys, fishbone diagrams, fault tree analysis), identifying the root cause, developing corrective actions and verifying their effectiveness. The template provides a repeatable framework that ensures investigations are thorough, objective, evidence-based and documented.
Root cause analysis is used across every industry where understanding why something went wrong is essential for preventing recurrence. In manufacturing, it investigates product defects and process failures. In healthcare, it analyses adverse events and near misses. In construction and mining, it examines safety incidents and equipment failures. In quality management systems such as ISO 9001, it forms the investigation component of the corrective action process. Without a structured RCA approach, organisations tend to address only the visible symptoms of problems, implementing quick fixes that leave the underlying cause untouched. This results in recurring failures, repeated incidents, wasted resources and a gradual erosion of confidence in the organisation ability to manage quality and safety.
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Benefits of using this root cause analysis template
- Recurrence prevention: identifying and addressing the true root cause eliminates the underlying condition that caused the problem, rather than just treating symptoms.
- Structured investigation: the template provides a step-by-step framework that ensures investigators follow a logical, evidence-based process rather than jumping to conclusions.
- Consistent documentation: a standardised template ensures every investigation is documented with the same level of rigour, making it easier to compare, review and learn from past investigations.
- Compliance support: a documented RCA process satisfies the investigation requirements of ISO 9001:2026 clause 10.2, WHS legislation, industry regulations and customer quality requirements.
- Knowledge capture: completed RCA documents capture organisational knowledge about failure modes, contributing factors and effective countermeasures that can be referenced for future investigations.
- Accountability: clear assignment of corrective actions to named individuals with due dates and effectiveness verification ensures that investigation findings translate into actual improvements.
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What to include in a root cause analysis template
This root cause analysis template covers 8 key areas:
- Investigation header: unique RCA reference number, investigation title, date of event, date investigation initiated, lead investigator name, investigation team members and investigation status (open, in progress, awaiting verification, closed).
- Problem statement: clear, factual description of what happened, when it happened, where it happened, who was affected, the magnitude or severity of the impact and the immediate consequences.
- Evidence collection: list of evidence gathered during the investigation, including photographs, measurements, process records, equipment logs, maintenance records, training records, witness statements and environmental data.
- Timeline reconstruction: chronological sequence of events leading up to, during and after the incident, with times, actions, decisions and conditions recorded to establish the chain of events.
- 5 Whys analysis: iterative questioning starting from the problem statement, asking "why" at each level until the root cause is reached (typically five to seven iterations, though the actual number depends on the complexity).
- Fishbone (Ishikawa) diagram: categorised analysis of contributing factors across people, process, equipment, materials, environment and management system categories.
- Root cause statement: concise statement of the identified root cause, supported by evidence from the investigation, distinguishing the root cause from contributing factors.
- Corrective action plan: specific actions to eliminate the root cause, responsible person for each action, due dates, resources required, changes to procedures or controls, and effectiveness verification method and date.
How to use this root cause analysis template
- Define the problem clearly, assemble the investigation team and collect all available evidence before beginning the analysis.: Write a clear, factual problem statement that describes what happened, when, where, who was affected and the severity of the impact. Avoid assumptions, opinions or premature conclusions. Assemble an investigation team that includes people with knowledge of the process, equipment or system involved. Collect all available evidence including photographs, process data, equipment logs, maintenance records, training records and witness statements. Preserve physical evidence where relevant.
- Reconstruct the timeline of events and identify the sequence of actions, decisions and conditions that led to the incident.: Map out the chronological sequence of events from normal operating conditions through to the incident and its immediate aftermath. Include times, actions taken by each person, decisions made, equipment states, environmental conditions and any deviations from normal procedures. Identify the points where the sequence diverged from the expected or planned path. The timeline often reveals contributing factors that are not immediately obvious from the problem statement alone.
- Apply structured analysis methods (5 Whys, fishbone diagram or both) to identify contributing factors and drill down to the root cause.: Start the 5 Whys analysis from the problem statement and ask "why" at each level, following the chain of causation until you reach a cause that can be directly addressed. If multiple causal chains exist, follow each one. Use a fishbone diagram to categorise contributing factors across people, process, equipment, materials, environment and management system categories. The root cause is typically a systemic issue such as an inadequate procedure, missing control, insufficient training, design flaw or management system gap, rather than individual human error.
- Document the root cause statement, distinguishing it from contributing factors, and develop corrective actions that specifically address the root cause.: Write a concise root cause statement that is supported by the evidence collected during the investigation. Contributing factors that increased the likelihood or severity of the incident should be documented separately but also addressed. Develop corrective actions that specifically eliminate the root cause, not just the symptoms. For each action, define what will be done, who is responsible, the due date, the resources required and any changes to procedures, training, equipment or controls.
- Implement corrective actions, verify their effectiveness after an appropriate period and close the investigation with lessons learned documented.: Implement each corrective action by the assigned due date and record the completion evidence. After an appropriate verification period (typically 30 to 90 days), assess whether the corrective action has been effective by reviewing whether the problem has recurred, whether similar issues have been prevented and whether the intended improvement is sustained. Document lessons learned and share them with relevant teams. Close the investigation with sign-off from the lead investigator and the accountable manager.
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Get the free templateEnter your email above to download the full root cause analysis template as a PDF.Back to download formHow often should you complete this report?
Root cause analysis is conducted in response to specific events rather than on a fixed schedule. Every significant non-conformance, safety incident, near miss, equipment failure, customer complaint or quality escape should trigger an RCA investigation. The depth and rigour of the investigation should be proportional to the severity and potential consequences of the event. Critical incidents (injuries, regulatory breaches, major quality failures) warrant a full team-based RCA within days. Major non-conformances should be investigated within two weeks. Minor issues may be investigated using a simplified 5 Whys approach.
Organisations should review their RCA register at least monthly to monitor open investigations, track corrective action completion and identify recurring themes. Quarterly management reviews should include a summary of RCA findings, trends and systemic issues identified. An annual review of the RCA programme itself, assessing investigation quality, timeliness and effectiveness of corrective actions, helps drive continuous improvement of the investigation process.
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Frequently asked questions
Applicable regulatory standards
This template is a starting point. Check the current requirements that apply to your equipment, work and location. The template alone does not establish compliance.
| Standard | Edition | Clauses this template relies on | Source |
|---|---|---|---|
| Quality management systems - RequirementsNonconformity and corrective action: eliminating causes and reviewing whether corrective action worked. | ISO 9001:2026 (Edition 6, published 16 September 2026) |
| International Organization for Standardization (ISO)Sold by the publisher |
| Occupational health and safety management systems - Requirements with guidance for useIncident, nonconformity and corrective action in an OH&S management system, including investigating causes. | ISO 45001:2018 (Edition 1) with Amd 1:2024 (climate action changes) |
| International Organization for Standardization (ISO)Sold by the publisher |
| Model Work Health and Safety RegulationsControls must be reviewed when they fail to control a risk. The model WHS laws set no express duty to investigate. | Model WHS Regulations as at 5 December 2025 (cited within as the Work Health and Safety Regulations 2011) |
| Safe Work Australia (drafted by the Parliamentary Counsel's Committee) |
| Model Work Health and Safety Act (Model Work Health and Safety Bill)Notifiable incidents go to the regulator immediately, with a record kept for at least 5 years. | Model WHS Bill as at 5 December 2025 (includes the Model WHS Legislation Amendment (Incident Notification) 2025) |
| Safe Work Australia (drafted by the Parliamentary Counsel's Committee) |
| Quality management systems - RequirementsAustralian and New Zealand identical adoption of ISO 9001:2026. | AS/NZS ISO 9001:2026 | Whole instrument | Standards Australia and Standards New ZealandSold by the publisher |
Quality management systems - Requirements
Edition: ISO 9001:2026 (Edition 6, published 16 September 2026)
Nonconformity and corrective action: eliminating causes and reviewing whether corrective action worked.
- 10.2: Nonconformity and corrective action.
International Organization for Standardization (ISO)Sold by the publisher
Occupational health and safety management systems - Requirements with guidance for use
Edition: ISO 45001:2018 (Edition 1) with Amd 1:2024 (climate action changes)
Incident, nonconformity and corrective action in an OH&S management system, including investigating causes.
- 10.2: Incident, nonconformity and corrective action, including investigation of causes.
International Organization for Standardization (ISO)Sold by the publisher
Model Work Health and Safety Regulations
Edition: Model WHS Regulations as at 5 December 2025 (cited within as the Work Health and Safety Regulations 2011)
Controls must be reviewed when they fail to control a risk. The model WHS laws set no express duty to investigate.
- reg 38: Control measures must be reviewed and revised as necessary, including when they fail, before changes creating new risks, for new hazards, after consultation, or on a qualifying representative's request.
- Part 3.1: Managing risks to health and safety: identify hazards, eliminate or minimise risks using the hierarchy of controls, maintain and review controls.
Safe Work Australia (drafted by the Parliamentary Counsel's Committee)
Model Work Health and Safety Act (Model Work Health and Safety Bill)
Edition: Model WHS Bill as at 5 December 2025 (includes the Model WHS Legislation Amendment (Incident Notification) 2025)
Notifiable incidents go to the regulator immediately, with a record kept for at least 5 years.
- s 38: A PCBU must notify the regulator immediately after becoming aware of a notifiable incident, by the fastest possible means, by telephone or in writing.
- s 38(7): A PCBU must keep a record of each notifiable incident for at least 5 years from the day notice of it was given to the regulator.
Safe Work Australia (drafted by the Parliamentary Counsel's Committee)
Quality management systems - Requirements
Edition: AS/NZS ISO 9001:2026
Australian and New Zealand identical adoption of ISO 9001:2026.
Standards Australia and Standards New ZealandSold by the publisher
Each source was read at its publisher and the page checked on 26 October 2026. The publisher's current text is the authority.
Root cause analysis template preview

The numbers behind this root cause analysis template
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Run an industry blog, trade association site, or training resource? Drop a preview of this free root cause analysis template straight into your page. The snippet is self-contained, needs no scripts, and links readers back to the full free template.
<div style="max-width:480px;font-family:system-ui,-apple-system,'Segoe UI',Roboto,sans-serif;border:1px solid #E5E7EB;border-radius:12px;padding:20px;background:#ffffff;">
<p style="font-size:12px;font-weight:700;letter-spacing:0.05em;text-transform:uppercase;color:#071D49;margin:0;">Free template</p>
<p style="font-size:18px;font-weight:700;color:#071D49;margin:6px 0 0;">Root cause analysis template</p>
<ul style="margin:12px 0 0;padding-left:18px;color:#374151;font-size:14px;line-height:1.6;">
<li style="margin:4px 0;">Investigation header: unique RCA reference number, investigation title, date of event, date investigation initiated, lead investigator name, investigation team members and investigation status (open, in progress, awaiting verification, closed).</li>
<li style="margin:4px 0;">Problem statement: clear, factual description of what happened, when it happened, where it happened, who was affected, the magnitude or severity of the impact and the immediate consequences.</li>
<li style="margin:4px 0;">Evidence collection: list of evidence gathered during the investigation, including photographs, measurements, process records, equipment logs, maintenance records, training records, witness statements and environmental data.</li>
<li style="margin:4px 0;">Timeline reconstruction: chronological sequence of events leading up to, during and after the incident, with times, actions, decisions and conditions recorded to establish the chain of events.</li>
<li style="margin:4px 0;">5 Whys analysis: iterative questioning starting from the problem statement, asking "why" at each level until the root cause is reached (typically five to seven iterations, though the actual number depends on the complexity).</li>
<li style="margin:4px 0;">Fishbone (Ishikawa) diagram: categorised analysis of contributing factors across people, process, equipment, materials, environment and management system categories.</li>
</ul>
<p style="font-size:13px;color:#6B7280;margin:14px 0 0;padding-top:12px;border-top:1px solid #E5E7EB;">Free <a href="https://www.maptrack.com/templates/root-cause-analysis-template" style="color:#071D49;font-weight:600;text-decoration:none;">Root cause analysis template</a> by MapTrack</p>
</div>Free to reuse, including commercially. This template is published under a Creative Commons Attribution 4.0 licence. Copy it, adapt it, put it on your own site or in your own docs. All we ask is that you credit MapTrack with a link back to this page. The snippet above already includes that credit, so if you use it as-is you’re covered.
Cite this template
Writing about this topic? You’re welcome to quote this checklist. Here’s the wording to use so your readers can find the original.
The MapTrack root cause analysis template has 3 columns and room for 4 entries.
- Short attribution
- MapTrack Root cause analysis template, https://www.maptrack.com/templates/root-cause-analysis-template
- Reference list
- MapTrack. (2026). Root cause analysis template [Checklist template]. Retrieved from https://www.maptrack.com/templates/root-cause-analysis-template
Free to reuse with credit under a Creative Commons Attribution 4.0 licence. If you’d rather link straight to it, the page is https://www.maptrack.com/templates/root-cause-analysis-template.
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