RecallHawk

Summary

CPSC recall: DIY Sauna Heater Kits. By Plunge Buddy LLC, doing business as DIY Cold Plunge, of North Mankato, Minnesota. Hazard: Electrical conductors within the sauna heater kits can overheat, posing a fire hazard and risk of serious injury or death.. Remedy: Consumers should stop using the recalled Sauna Heater Kit immediately and register at www.diycoldplunge.com/pages/recall for a full refund. Consumers will be asked to submit written and photo proof that the product has been destroyed/dispo

Details

Source

CPSC Consumer Product Recall

External ID

10679

Action Date

2026-03-26

Status

Recalled

Category

consumer_product

Product Description

This recall involves the DIY Sauna Heater Kit. The product is a do-it-yourself kit for consumers to assemble a heating f

Context & Analysis

This is a unclassified recall.

This was one of 20 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Plunge Buddy LLC, doing business as DIY Cold Plunge, of North Mankato, Minnesota 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 (Plunge Buddy LLC, doing business as DIY Cold Plunge, of North Mankato, Minnesota) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Plunge Buddy LLC, doing business as DIY Cold Plunge, of North Mankato, Minnesota have FDA actions?

Plunge Buddy LLC, doing business as DIY Cold Plunge, of North Mankato, Minnesota 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 "10679" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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