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Consumer Product Safety

Incident Report

Subform I: General Information

1. Report Type.

New incident report

Incident Report Number: 2019-4800

2. Registrant Information.

Registrant Reference Number: ProPharma Group case #: 1-57339166

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

Address: 140 Research Lane, Research Park

City: Guelph

Prov / State: Ontario

Country: Canada

Postal Code: N1G4Z3

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

Domestic Animal

4. Date registrant was first informed of the incident.

15-JUL-19

5. Location of incident.

Country: UNITED STATES

Prov / State: ILLINOIS

6. Date incident was first observed.

15-JUL-19

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.       PMRA Submission No.       EPA Registration No. 100-1247

Product Name: CRUISERMAXX

  • Active Ingredient(s)
    • FLUDIOXONIL
      • Guarantee/concentration 1.12 %
    • METALAXYL-M (MEFENOXAM)
      • Guarantee/concentration 1.7 %
    • THIAMETHOXAM
      • Guarantee/concentration 22.61 %

PMRA Registration No.       PMRA Submission No.       EPA Registration No. 100-1561

Product Name: VIBRANCE MAXX

  • Active Ingredient(s)
    • FLUDIOXONIL
      • Guarantee/concentration 2.35 %
    • METALAXYL-M (MEFENOXAM)
      • Guarantee/concentration 3.52 %
    • SEDAXANE
      • Guarantee/concentration 4.69 %

7. b) Type of formulation.

Other (specify)

treated seed corn

Application Information

8. Product was applied?

No

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 III: Domestic Animal Incident Report

1. Source of Report

Animal's Owner

2. Type of animal affected

Cow / Vache

3. Breed

Unknown

4. Number of animals affected

1

5. Sex

Unknown

6. Age (provide a range if necessary )

Unknown

7. Weight (provide a range if necessary )

Unknown

8. Route(s) of exposure

Oral

Unknown

9. What was the length of exposure?

Unknown / Inconnu

10. Time between exposure and onset of symptoms

Unknown / Inconnu

11. List all symptoms

System

  • General
    • Symptom - Death

12. How long did the symptoms last?

Persisted until death

13. Was medical treatment provided? Provide details in question 17.

Unknown

14. a) Was the animal hospitalized?

Unknown

14. b) How long was the animal hospitalized?

15. Outcome of the incident

Died

16. How was the animal exposed?

Accidental ingestion/Ingestion accident.

17. Provide any additional details about the incident

(eg. description of the frequency and severity of the symptoms

1-57339166- The reporter, a livestock owner, indicates an exposure to two pesticide products containing the active ingredients thiamethoxam, fludioxonil, metalaxyl-m (mefenoxam), and sedaxane. One day before the day of initial contact with the registrant, the reporter indicated his cow of unknown age, breed, weight and gender had ingested an unknown amount of the product, then died on the day of initial contact. No additional information is available.


To be determined by Registrant

18. Severity classification (if there is more than 1 possible classification

Death

19. Provide supplemental information here