Product Withdrawal Record
Professional, ready-to-use QEHS document designed to support effective implementation, documentation, and ongoing compliance with applicable management system requirements.
- Standard
- ISO 22000
- Document Type
- Records
- Format
- DOCX
- Language
- English
- Tags
- FSMS, ISO 22000, Records
This record is used by your organisation to document each withdrawal or recall of end products identified as potentially unsafe, as required by Clause 8.9.5 of ISO 22000:2018. It records the decision, the people with authority, notifications to interested parties, the products and quantities affected and recovered, the handling of recovered product, the root cause and the verification of effectiveness.
What's Inside
- Withdrawal / Recall Team and Authority
- Withdrawal Record
- Initiation and Decision
- Notifications (8.9.5 b)
- Product Accounting
- Handling of Recovered Product (8.9.5 c)
- Cause, Corrective Action and Closure
- Withdrawal and Recall Log
ISO 22000 Alignment
Supports ISO 22000:2018 requirements, including Clause 8.9.5. It fits with the rest of the QEHS Vault ISO 22000 document set.
Format
Supplied as a fully editable Microsoft Word (.docx) file. Add your organisation’s name, logo and details, then use it straight away. Instant download after purchase.
Key Benefits
- Professional, ready-to-use QEHS document designed to support effective implementation, documentation, and ongoing compliance with applicable management system requirements
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