ISO 13485 / MDR document template:

Registry of Recalled / Withdrawn Products

The purpose of this record is to give an overview of all recalls and withdrawals that the organization performed. It can also be used as an input for analyzing the QMS and making imporvements.

The document is optimized for small and medium-sized organizations - we believe that overly complex and lengthy documents are just overkill for you.

This document is an appendix to the main document, which is sold separately: Procedure for Control of Non-Conforming Products.

RELATED DOCUMENTS Related-Documents-Arrow Procedure for Control of Nonconforming Products Related-Documents-Arrow Nonconforming Product Record Related-Documents-Arrow Registry of Nonconformities
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RELATED DOCUMENTS Related-Documents-Arrow Procedure for Control of Nonconforming Products Related-Documents-Arrow Nonconforming Product Record Related-Documents-Arrow Registry of Nonconformities

DOCUMENT FEATURES

OVERVIEW

  • Price
    US$ 19.90
  • Compliant with
    ISO 13485 clause 8.3.3
  • Format
    MS Word 2013, MS Word 2016, MS Word 2019
  • Number of pages
    1
  • Document language
    English

USABILITY

  • Can I edit the document?
    Yes. The document is fully editable – just enter information specific to your company.
  • Can I use this to become certified?
    Yes. The documentation template may be used for ISO 13485 certification audit purposes.
  • Well-defined instructions
    Document templates contain an average of twenty comments each, and offer clear guidance for filling them out.
  • Designed with your company in mind
    The template was created for small and medium-sized businesses.
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WHAT OUR CUSTOMERS SAY ABOUT US

The documents are well laid out and with our company’s standard formatting they are just falling into place.

Thomas Green

CBCP

Simple gave us an example of how the document could be structured and the different fields to include. Helped us not leave anything out.

Wynn Johansson-Nunez

SVENSKA DENTORAMA AB.

OUR CLIENTS

Registry of Recalled / Withdrawn Products - 13485Academy
Registry of Recalled / Withdrawn Products - 13485Academy
Registry of Recalled / Withdrawn Products - 13485Academy
Registry of Recalled / Withdrawn Products - 13485Academy
Registry of Recalled / Withdrawn Products - 13485Academy
Registry of Recalled / Withdrawn Products - 13485Academy

Preview Registry of Recalled / Withdrawn Products template

  • The document is fully editable so that you can adapt it to your company design.
  • Documents include placeholder marks for all information you need to complete.
  • Each document includes comments and information, which guides you through completion.
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