version: 2
sources:
- name: fda_device_recalls
  description: FDA Device Recall Reports Sample discovered from api.fda.gov. Bounded
    source query (limit=100); completeness is not assumed.
  meta:
    opendataodc:
      dataset_id: fda-device-recalls
      revision_id: 20260907135529-a7cd5d0f3305
      detected_at: '2026-09-07T13:55:29+00:00'
      source_url: https://api.fda.gov/device/recall.json?limit=100
  tables:
  - name: recall_json
    description: Source asset recall.json.
    meta:
      opendataodc:
        source_url: https://api.fda.gov/device/recall.json?limit=100
        content_hash: d7351bbcbb39cb42bfae873fb6cccc2cf5d72d115d3624525328258d7ffba040
        row_count: 100
        parser_errors:
        - 'Partial response: 100 of 59102 provider records'
    columns:
    - name: action
    - name: additional_info_contact
    - name: address_1
    - name: address_2
    - name: cfres_id
    - name: city
    - name: code_info
    - name: country
    - name: distribution_pattern
    - name: event_date_created
    - name: event_date_initiated
    - name: event_date_posted
    - name: event_date_terminated
    - name: firm_fei_number
    - name: k_numbers
    - name: openfda
    - name: pma_numbers
    - name: postal_code
    - name: product_code
    - name: product_description
    - name: product_quantity
    - name: product_res_number
    - name: reason_for_recall
    - name: recall_status
    - name: recalling_firm
    - name: res_event_number
    - name: root_cause_description
    - name: state