RecallHawk

Super Lube Syncopen Synthetic Penetrant, Super Lube Fire Resistant Hydraulic Fluid, and Super Lube Metal Protectant and

Kano Laboratories LLC, of Bohemia, New York

Summary

CPSC recall: Super Lube Syncopen Synthetic Penetrant, Super Lube Fire Resistant Hydraulic Fluid, and Super Lube Metal Protectant and Corrosion Inhibitor (consumer sizes of five gallons or less). By Kano Laboratories LLC, of Bohemia, New York. Hazard: The recalled products contain either ethylene glycol or low-viscosity petroleum distillates, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The packaging for the products is not child resistant

Details

Source

CPSC Consumer Product Recall

External ID

9956

Action Date

2024-05-16

Status

Recalled

Category

consumer_product

Product Description

The recall involves Super Lube products which include the following: Syncopen Synthetic Penetrant, Fire Resistant Hydrau

Context & Analysis

This is a unclassified recall.

This was one of 11 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Kano Laboratories LLC, of Bohemia, New York has 2 FDA actions in our database, including 1 recall.

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 (Kano Laboratories LLC, of Bohemia, New York) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Kano Laboratories LLC, of Bohemia, New York have FDA actions?

Kano Laboratories LLC, of Bohemia, New York has 2 FDA actions in our database, including 1 recall and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9956" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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