MCA MCA-F-303MCA-F-303/02, 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-303/02, version 2 is the official MCA identifier for “Recall Report Form — version 2, 01 July 2020”. MCA-F-303/02, version 2 is the official identifier MCA uses for this instrument.
- Instrument
- MCA-F-303
- Full name
- MCA-F-303/02, 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 Report Form — version 2, 01 July 2020
Complete one-page recall-report form covering distribution, returned and outstanding stock, consignee replies and disposal. Existing MCA-GL-303 paragraph2.2 includes medical devices and paragraph7.1 references the reporting form. Its dosage/ingredient fields remain literal source fields; no pharmaceutical-only exclusion or generic device adaptation is inferred. Printed version date does not establish statutory commencement. Later instruments, current implementing lists and continued applicability remain under review.
MCA-F-303/02, 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.