# Enable Remedial Actions and Malfunction for Combination Products

Veeva Safety now supports data entry for remedial actions and malfunctions at the device-level, as well as device codes for _Cases_ that involve multiple _Combination Products_ or a _Combination Product_ that has multiple device constituents. Vault exports _Remedial Actions_ and _Malfunctions_ on _Case Products_ to FDA Medwatch 3500A, FDA E2B(R2), and FDA VAERS E2B(R3) formats.

For details on working with device-specific adverse event codes, see <a href="/en/lr/01331/">Enable the IMDRF Dictionary for Maintenance, Case Processing, and Submissions</a>.

After configuring this feature, see more information about entering remedial actions and malfunctions at the <a href="/en/lr/01287/#device-manufacturer-analysis-fields">_Case Product_ level</a> and the <a href="/en/lr/01287/#report-details">_Case_ level</a>.

## Update Case Page Layout for Device Report Type (Status)

1. Navigate to **Admin > Configuration > Objects > Case > Layouts > Case Page Layout**.
2. In the **Device Details** section, complete the following setup:
    * Add the **Device Report Type (Status)** field.
    * Remove the **Remedial Action** and **Remedial Action-Other** fields.
3. To rearrange the fields, drag and drop.
4. Select **Save**.

## Update Case Product Device Detail Page Layout for Remedial Action and Malfunction

1. Navigate to **Admin > Configuration > Objects > Case Product > Layouts > Device Detail Page Layout**.
2. In the **Details** section, complete the following setup:
    * Add the **Malfunction** field.
    * Add the **Remedial Action** field.
    * Add the **Remedial Action Other** field.
3. To rearrange the fields, drag and drop.
4. Select **Save**.