Recall - CISMeF

Preferred Label : Recall;

NCIt definition : A removal or correction of a marketed product that the FDA considers to be in violation of the laws it administers and against which the agency would initiate legal action, such as seizure. A recall may be a voluntary action conducted by the manufacturer, by FDA request, or by FDA order under statutory authority.;

Details

Origin ID

C53609;

UMLS CUI

C1705180;

Automatic exact mappings (from CISMeF team)
- Recall [LOINC component]
- Recalled product [MedDRA Preferred Term]
- Recalls [IAB term]
- Reminding (procedure) [SNOMED CT concept]
- callback [Radlex concept]
- memory, short-term [MeSH Descriptor]
- mental recall [MeSH Descriptor]
- product recalls [MeSH concept]
- product recalls and withdrawals [MeSH Descriptor]
Semantic type(s)
- Governmental or Regulatory Activity [UMLS semantic type]
concept_is_in_subset
- FDA Individual Case Safety Report Terminology [NCIt concept]
- Type of Remedial Action ICSR Terminology [NCIt concept]

Keyword's position in hierarchy(ies) :

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