MCA MCA-F-303MCA-F-303/01, Version 2
Currentness under review. Whether this instrument remains applicable is under review. Consult the later instruments and source context below before relying on it.
MCA-F-303/01, Version 2 is the official MCA identifier for “Recall Information Form (Parts 1 and 2) — version 2, 01 July 2020”. MCA-F-303/01, Version 2 is the official identifier MCA uses for this instrument.
- Instrument
- MCA-F-303
- Full name
- MCA-F-303/01, Version 2
- Category
- Vigilance
- Source publication
- English
- Readable HTML
- 1 language version
- Published
- —
- Effective
- —
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Each version has stable passage anchors for direct citations and highlighting. The readable text is generated from an authority source and does not replace the legally controlling publication.
Recall Information Form (Parts 1 and 2) — version 2, 01 July 2020
Complete three-page authority recall-information form covering defect details, product/distribution information, risk assessment and proposed action. Existing MCA-GL-303 paragraph2.2 expressly includes faulty/nonperforming medical devices and paragraph7.1 references the form. Pharmaceutical-style fields remain source fields; device-specific adaptation and later revisions remain unresolved. The printed version date is not treated as legal commencement. Later instruments, current implementing lists and continued applicability remain under review.
MCA-F-303/01, Version 2 is the official identifier MCA uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.