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Incident Report

Subform I: General Information

1. Report Type.

New incident report

Incident Report Number: 2025-1502

2. Registrant Information.

Registrant Reference Number: M-159680-01-1

Registrant Name (Full Legal Name no abbreviations): BAYER CROPSCIENCE INC.

Address: 160 QUARRY PARK BOULEVARD SE SUITE 130

City: CALGARY

Prov / State: AB

Country: CANADA

Postal Code: T2C 3G3

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. 24563      PMRA Submission No.       EPA Registration No.

Product Name: FOSETYL-AL TECHNICAL

• Active Ingredient(s)
  • FOSETYL-ALUMINUM

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 Efosit Al: Sub-acute inhalation toxicity in rats (14 x 6 hour exposures)

Date 02-OCT-79

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

No

3. Type of incident identified in the study

New health or environmental hazard

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)

A sub-acute inhalation toxicity study with fosetyl-Al in rats was conducted. There were mortalities in the high dose group, and treatment-related histopathological effects in the respiratory tract in all groups in a dose-dependent manner. A no-effect levels was not established in the study.

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?

For Registrant use only

7. Provide supplemental information here