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Incident Report

Subform I: General Information

1. Report Type.

Update the report

Incident Report Number: 2010-4955

2. Registrant Information.

Registrant Reference Number: 2010-51

Registrant Name (Full Legal Name no abbreviations): Monsanto Canada Inc.

Address: 180 Kent Street, Suite 810

City: Ottawa

Prov / State: ON

Country: Canada

Postal Code: K1P 0B6

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. 28965      PMRA Submission No.       EPA Registration No.

Product Name: DICAMBA TECHNICAL HERBICIDE

• Active Ingredient(s)
  • DICAMBA (PRESENT AS ACID, AMINE SALT, ESTER, OR SODIUM SALT)

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 A 24-MONTH ORAL (DIET) COMBINED CHRONIC TOXICITY/CARCINOGENICITY STUDY IN RATS

Date 06-SEP-10

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)

Non-statistically significant increase of polyps at two highest test rates.

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?

31-DEC-10

For Registrant use only

7. Provide supplemental information here

This finding fell within laboratory historical control data and it is believed this finding does not change or have an impact on the current endpoints or risk assessment outcomes established for the regulation of dicamba.