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Incident Report

Subform I: General Information

1. Report Type.

New incident report

Incident Report Number: 2014-1201

2. Registrant Information.

Registrant Reference Number: 2014-10

Registrant Name (Full Legal Name no abbreviations): BASF Canada

Address: 100 Milverton

City: Mississauga

Prov / State: ON

Country: Canada

Postal Code: ON

3. Select the appropriate subform(s) for the incident.

Scientific Study

4. Date registrant was first informed of the incident.

5. Location of incident.

6. Date incident was first observed.

Product Description

7. a) Provide the active ingredient and, if available, the registration number and product name (include all tank mixes). If the product is not registered provide a submission number.

PMRA Registration No. 30561      PMRA Submission No.       EPA Registration No.

Product Name: Xemium

• Active Ingredient(s)
  • FLUXAPYROXAD

PMRA Registration No.       PMRA Submission No.       EPA Registration No.

Product Name: PYRACLOSTROBIN

• Active Ingredient(s)
  • PYRACLOSTROBIN

PMRA Registration No.       PMRA Submission No.       EPA Registration No.

Product Name: EPOXICONAZOLE

• Active Ingredient(s)
  • EPOXICONAZOLE

7. b) Type of formulation.

Application Information

8. Product was applied?

Unknown

9. Application Rate.

10. Site pesticide was applied to (select all that apply).

11. Provide any additional information regarding application (how it was applied, amount applied, the size of the area treated etc).

To be determined by Registrant

12. In your opinion, was the product used according to the label instructions?

Unknown

Subform VII: Scientific Study

1. Study Reference

Title Daphnia acute

Date 07-APR-14

2. a) Is an extension needed to translate the document?

No

3. Type of incident identified in the study

Increased health or environmental risk

4. Describe the incident identified in the study (e.g. study demonstrates an increased risk to non-Hodgkin's Lymphoma after exposure to pesticide X)

Daphnia test of new formulation incl ai registered in Canada

5. a) Was the study discontinued before completion?

No

5. b) Provide the reason for discontinuation

6. If the study is ongoing, what is the expected completion date?

Unknown

For Registrant use only

7. Provide supplemental information here

Formulation experimental, may not be relevant