Incident Report
Subform I: General Information
1. Report Type.
New incident report
Incident Report Number: 2011-0843
2. Registrant Information.
Registrant Reference Number: PROSAR CASE# 1-23046331
Registrant Name (Full Legal Name no abbreviations): Syngenta Crop Protection 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.
Human
4. Date registrant was first informed of the incident.
09-JUN-10
5. Location of incident.
Country: UNITED STATES
Prov / State: NEW JERSEY
6. Date incident was first observed.
Unknown
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. 100-1066
Product Name: Demand CS
- Active Ingredient(s)
- LAMBDA-CYHALOTHRIN
- Guarantee/concentration 9.7 %
PMRA Registration No.
PMRA Submission No.
EPA Registration No. 100-1004
Product Name: Demon EC
- Active Ingredient(s)
- CYPERMETHRIN
- Guarantee/concentration 25.3 %
PMRA Registration No.
PMRA Submission No.
EPA Registration No. Unknown
Product Name: Talon G (non-specific)
- Active Ingredient(s)
- BRODIFACOUM
- Guarantee/concentration .005 %
7. b) Type of formulation.
Liquid
Bait
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 II: Human Incident Report (A separate form for each person affected)
1. Source of Report.
Other
2. Demographic information of data subject
Sex: Male
Age: Unknown / Inconnu
3. List all symptoms, using the selections below.
System
4. How long did the symptoms last?
Persisted until death
5. Was medical treatment provided? Provide details in question 13.
Unknown
6. a) Was the person hospitalized?
Unknown
6. b) For how long?
7. Exposure scenario
Occupational
8. How did exposure occur? (Select all that apply)
9. If the exposure occured during application or re-entry, what protective clothing was worn? (select all that apply)
Unknown
10. Route(s) of exposure.
Skin
Respiratory
11. What was the length of exposure?
Unknown / Inconnu
12. Time between exposure and onset of symptoms.
Unknown / Inconnu
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.)
1-23046331- The registrant was notified through litigation of possible exposure to three pesticide products containing the active ingredients, lambda-cyhalothrin, cypermethrin, and brodifacoum. Initially when the registrant was informed (06/09/10) it was unclear which products were involved and reporting was not possible. Updated documentation 12/20/10 facilitated reporting. The proposed exposure had taken place in occupational setting (unknown occupation). A male (unknown demographics) was reported to have been exposed on a daily basis to the listed products via inhalation, dermal contact, as well as żżżother means? (not clarified). No discreet exposure incident was described. The exposure was reported to have taken place between 10/--/96 and 12/--/07. The exposed individual is reported to be deceased (unknown time of death, unknown cause). No further information is available at this time.
To be determined by Registrant
14. Severity classification.
Death
15. Provide supplemental information here.