RecallHawk

Liquefied Petroleum Gas Compact Regulators

Engineered Controls International LLC, of Elon, North Carolina

Summary

CPSC recall: Liquefied Petroleum Gas Compact Regulators. By Engineered Controls International LLC, of Elon, North Carolina. Hazard: The regulators could leak gas, posing a fire hazard.. Remedy: Consumers should immediately stop using the recalled regulators, turn off the propane cylinder valve, and disconnect the regulator. Consumers should contact their RegO distributor or RegO to receive a free replacement regulator. Consumers should discard the recalled regulator..

Details

Source

CPSC Consumer Product Recall

External ID

9704

Action Date

2023-09-07

Status

Recalled

Category

consumer_product

Product Description

This recall involves the RegO 302 Series Compact Regulators with dates codes between 09/22 and 02/23. Regulators with th

Context & Analysis

This is a unclassified recall.

This was one of 13 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Engineered Controls International LLC, of Elon, North Carolina 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 (Engineered Controls International LLC, of Elon, North Carolina) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Engineered Controls International LLC, of Elon, North Carolina have FDA actions?

Engineered Controls International LLC, of Elon, North Carolina 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 "9704" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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