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Consumer Product Safety

Incident Report

Subform I: General Information

1. Report Type.

New incident report

Incident Report Number: 2022-0827

2. Registrant Information.

Registrant Reference Number: M-600983-02-1

Registrant Name (Full Legal Name no abbreviations): Bayer CropScience Inc.

Address: Suite 200, 160 Quarry Park Boulevard SE

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.

Active(s)

PMRA Registration No. 30221      PMRA Submission No.       EPA Registration No.

Product Name: INDAZIFLAM 200 SC HERBICIDE

  • Active Ingredient(s)
    • INDAZIFLAM

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 Toxicity of Indaziflam SC 200 to Duckweed (Lemna gibba G3) Under Static-Renewal Conditions

Date 12-SEP-17

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)

A Lemna gibba (duckweed) study using a 200 SC formulation of indaziflam was conducted for a submission in the European Union. While the EC50 generated does not meet the adverse effect reporting criteria, the study yielded an undefined NOEC lower than was obtained that with previous Lemna gibba testing.

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

The NOEC is not used by PMRA to assess risk to aquatic plants, so this finding should have no impact on the risk assessment.