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Consumer Product Safety

Incident Report

Subform I: General Information

1. Report Type.

New incident report

Incident Report Number: 2013-6701

2. Registrant Information.

Registrant Reference Number: A130120053

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

Address: Suite 2100, 450 - 1 Street S.W.

City: Calgary

Prov / State: Alberta

Country: Canada

Postal Code: T2P 5H1

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

Domestic Animal

4. Date registrant was first informed of the incident.

27-AUG-13

5. Location of incident.

Country: UNITED STATES

Prov / State: ARIZONA

6. Date incident was first observed.

20-AUG-13

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. 62719--537

Product Name: Milestone VM Herbicide

  • Active Ingredient(s)
    • AMINOPYRALID
      • Guarantee/concentration 40.6

PMRA Registration No.       PMRA Submission No.       EPA Registration No. Unknown

Product Name: Tri-4 Herbicide

  • Active Ingredient(s)

7. b) Type of formulation.

Liquid

Application Information

8. Product was applied?

Yes

9. Application Rate.

Unknown

10. Site pesticide was applied to (select all that apply).

Site: Other / Autre

Préciser le type: pasture

11. Provide any additional information regarding application (how it was applied, amount applied, the size of the area treated etc).

Exposure involved unknown amount orally . The exposure was yard use, and occurred at animal owner field/pasture. Caller has been using the product and some of the cows have become sick. Last use of the product was 3 days ago, but the caller had been using it off and on for 3-4 days.

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

Medical Professional

2. Type of animal affected

Cow / Vache

3. Breed

Bovine

4. Number of animals affected

2

5. Sex

Male

Female

6. Age (provide a range if necessary )

2

7. Weight (provide a range if necessary )

1200

lbs

8. Route(s) of exposure

Unknown

9. What was the length of exposure?

>3 days <=1 wk / >3 jours <=1 sem

10. Time between exposure and onset of symptoms

>3 days <=1 wk / >3 jours <=1 sem

11. List all symptoms

System

  • Nervous and Muscular Systems
    • Symptom - Ataxia
  • Eye
    • Symptom - Blindness (temporary)
  • Gastrointestinal System
    • Symptom - Stomach pain
    • Specify - abdominal pain
  • General
    • Symptom - Other
    • Specify - kicking at flank
    • Symptom - Death

12. How long did the symptoms last?

Unknown / Inconnu

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?

Contact treat.area/Contact surf. traitée

17. Provide any additional details about the incident

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

Caller has been using the product and some of the cows have become sick. Last use of the product was 3 days ago, but he had been using it off and on for 3-4 days. Exposure involved unknown amount orally . The exposure was yard use, and occurred at animal owner field/pasture. Both of these herbicides should not be a risk to grazing livestock, especially if the product has dried before they entered the pasture. There are no grazing restrictions for beef cattle with either product.


To be determined by Registrant

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

Death

19. Provide supplemental information here

Subform III: Domestic Animal Incident Report

1. Source of Report

Medical Professional

2. Type of animal affected

Cow / Vache

3. Breed

Bovine

4. Number of animals affected

1

5. Sex

Female

6. Age (provide a range if necessary )

6

7. Weight (provide a range if necessary )

1200

lbs

8. Route(s) of exposure

Oral

9. What was the length of exposure?

>3 days <=1 wk / >3 jours <=1 sem

10. Time between exposure and onset of symptoms

>3 days <=1 wk / >3 jours <=1 sem

11. List all symptoms

System

  • General
    • Symptom - Death

12. How long did the symptoms last?

Unknown / Inconnu

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

6.0 yr lactating female weighing 1200.0 lb. Was in good health previously. Exposure involved unknown amount orally . The exposure was yard use, and occurred at animal owner field/pasture. One cow died yesterday. He has seen some tumbleweeds in the pasture and there is Kochia that they could have ingested. It's very possible that the effects seen could have been a result of ingestion of Kochia plants, or it could be from nitrates. Asked about potential lead exposure, the caller said that it did cross his mind, since he did have cattle in the past that were exposed to an old battery and the symptoms observed were similar. There are no batteries in the pasture though, that he is aware of.


To be determined by Registrant

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

Death

19. Provide supplemental information here

Both of these herbicides should not be a risk to grazing livestock, especially if they were dried before they entered the pasture. There are no grazing restrictions for beef cattle with either product. Because the time course was poorly consistent, the amount was unknown consistent, and the findings were poorly consistent, this substance was considered to have low likelihood of causing the clinical situation.