New incident report
Incident Report Number: 2014-4957
Registrant Reference Number: 5287220
Registrant Name (Full Legal Name no abbreviations): Sure-Gro Inc.
Address: 1900 Minnesota Crt
City: Mississauga
Prov / State: Ontario
Country: Canada
Postal Code: L5N 3C9
Human
Country: CANADA
Prov / State: ONTARIO
PMRA Registration No. 26679 PMRA Submission No. EPA Registration No.
Product Name: HomeCare Bed Bug & Crawling Insect Killer Dust
Yes
Unknown
Site: Res. - In Home / Rés. - à l'int. maison
Unknown
Data Subject
Sex: Male
Age: >19 <=64 yrs / >19 <=64 ans
System
Unknown / Inconnu
Yes
No
Non-occupational
Contact with treated area
None
Oral
Unknown / Inconnu
>2 mos <=6 mos / > 2 mois < = 6 mois
Caller has been using the product liberally. The top of the callers soft pallet is tough. Caller has had a chronic sore throat and is trying to rule out if the product is causing callers symptoms. Caller takes copious amounts of water to relieve his throat irritation and takes chloraseptic to ease the irritation. Caller admits to being a smoker. Caller went to his ear, nose and throat doctor and they diagnosed him with irritation. Callers primary doctor had caller on two different antibiotics and had diagnosed caller with irritation also. gh, nka, meds: pain medications, tritratrol. R: Advised caller to ventilate the home until the dust odor is no longer there. Advised caller to always follow label instructions. Advised caller to wear PPE while cleaning his apartment. Advised caller to complete a steam inhalation treatment for relief. Advised caller to continue to follow his Doctors instructions if SX worsen or persist. Offered to call back to PC with any additional concerns. Caller declined PC to follow
Minor
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.