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Consumer Product Safety

Incident Report

Subform I: General Information

1. Report Type.

New incident report

Incident Report Number: 2021-2134

2. Registrant Information.

Registrant Reference Number: M-679477-01-1

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

Address: Suite 200, 160 Quarry Park Blvd S.E.

City: Calgary

Prov / State: Alberta

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. 33955      PMRA Submission No.       EPA Registration No.

Product Name: Propulse

  • Active Ingredient(s)
      • Guarantee/concentration 200 g/L
      • Guarantee/concentration 200 g/L

7. b) Type of formulation.

Application Information

8. Product was applied?


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?


Subform VII: Scientific Study

1. Study Reference

Title Fluopyram + prothioconazole SE 250 (125+125 g/L): Chronic Toxicity to the Honey Bee Apis mellifera L. under Laboratory Conditions

Date 27-FEB-20

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


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)

Lower chronic levels The chronic oral toxicity of Fluopyram + prothioconazole SE250 to adult honey bee (Apis mellifera) was investigated in a study performed in accordance with OECD No 245. The study reported a NOEDD of 37.6 g formulation/bee/day. This endpoint is lower than previously reported for fluopyram formulations.

5. a) Was the study discontinued before completion?


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

Formulation not registered in Canada but similar to registered formulation.