Incident Report
Subform I: General Information
1. Report Type.
New incident report
Incident Report Number: 2015-1693
2. Registrant Information.
Registrant Reference Number: 1471366
Registrant Name (Full Legal Name no abbreviations): Dow AgroSciences Canada Inc.
Address: 450-1st Street SW, Suite 2100
City: Calgary
Prov / State: AB
Country: Canada
Postal Code: T2P 5H1
3. Select the appropriate subform(s) for the incident.
Human
4. Date registrant was first informed of the incident.
26-SEP-14
5. Location of incident.
Country: CANADA
Prov / State: SASKATCHEWAN
6. Date incident was first observed.
26-SEP-14
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. 30914
PMRA Submission No.
EPA Registration No.
Product Name: CURTAIL M HERBICIDE (Canada)
- Active Ingredient(s)
- CLOPYRALID
- MCPA (PRESENT AS ESTERS)
7. b) Type of formulation.
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: Job site
11. Provide any additional information regarding application (how it was applied, amount applied, the size of the area treated etc).
Please refer to field 13 on Subform II or field 17 of subform III for a detailed description regarding application.
To be determined by Registrant
12. In your opinion, was the product used according to the label instructions?
Unknown
Subform II: Human Incident Report (A separate form for each person affected)
1. Source of Report.
Other
2. Demographic information of data subject
Sex: Female
Age: >19 <=64 yrs / >19 <=64 ans
3. List all symptoms, using the selections below.
System
4. How long did the symptoms last?
Unknown / Inconnu
5. Was medical treatment provided? Provide details in question 13.
Unknown
6. a) Was the person hospitalized?
No
6. b) For how long?
Unknown
7. Exposure scenario
Occupational
8. How did exposure occur? (Select all that apply)
What was the activity? Please refer to field 13 on Subform II or field 17 of subform III for a detailed description regarding the activity
Other
9. If the exposure occured during application or re-entry, what protective clothing was worn? (select all that apply)
None
10. Route(s) of exposure.
Unknown
11. What was the length of exposure?
<=15 min / <=15 min
12. Time between exposure and onset of symptoms.
<=30 min / <=30 min
13. Provide any additional details about the incident (eg. description of the frequency and severity of the symptoms, type of medical treatment, results from medical tests, outcome of the incident, amount of pesticide exposed to, etc.)
9/26/2014 Caller is calling for a co-worker who was sitting in the cab of a truck when the product was applied at a job site where they both work. The window in the truck was open with the air conditioner on when the product was applied nearby. The product was diluted according to the label recommendations, and was sprayed with a water volume of ten gallons to an acre. Co-worker is complaining of itching on her left arm and lower abdominal pain. Co-worker did not have any direct exposure, and she is pregnant.
To be determined by Registrant
14. Severity classification.
Minor
15. Provide supplemental information here.
The information contained in this report is based on self-reported statements provided to the registrant during telephone Interview(s). These self-reported descriptions of an incident have not been independently verified to be factually correct or complete descriptions of the incident. For that reason, information contained in this report does not and can not form the basis for a determination of whether the reported clinical effects are causally related to exposure to the product identified in the telephone interviews.