Pro Supply Outlet (PSO) Sodium and Potassium Hydroxide
Chemical Technologies International Inc., dba Pro Supply Outlet, of Rancho Cordova, Calif.
Summary
CPSC recall: Pro Supply Outlet (PSO) Sodium and Potassium Hydroxide. By Chemical Technologies International Inc., dba Pro Supply Outlet, of Rancho Cordova, Calif.. Hazard: The products contain sodium hydroxide or potassium hydroxide which must be in child resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant, posing a risk of chemical burns and irritation to the skin and eyes. In addition, the label on the product vio
Details
Source
CPSC Consumer Product Recall
External ID
9071
Action Date
2021-05-20
Status
Recalled
Category
consumer_product
Product Description
This recall involves Pro Supply Outlet sodium and potassium hydroxide products sold in two-pound rigid white plastic jar
Context & Analysis
This is a unclassified recall.
This was one of 9 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Frequently Asked Questions
What is a FDA recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Chemical Technologies International Inc., dba Pro Supply Outlet, of Rancho Cordova, Calif.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Chemical Technologies International Inc., dba Pro Supply Outlet, of Rancho Cordova, Calif. have FDA actions?
This is the only FDA action we have on record for Chemical Technologies International Inc., dba Pro Supply Outlet, of Rancho Cordova, Calif. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9071" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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