DIY Sauna Heater Kits
Plunge Buddy LLC, doing business as DIY Cold Plunge, of North Mankato, Minnesota
Summary
CPSC recalled 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/disposed of or request a prepaid shipping label to return the product..
Details
Source
cpsc
External ID
26349
Action Date
2026-03-26
Status
Ongoing
Category
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 fixture with four heat-lamp bulbs (sold separately) and a metal enclosure intended for use in a separate do-it-yourself sauna enclosure, for which carpentry plans are sold separately. The Sauna Heater Kit includes a stainless steel cage (which weighs about 16 lbs., and measures 12"H x 12"W x 8"D when assembled), screws/bolts for assembly, four ceramic bulb sockets, three wire connectors, two ground pigtails, and a three-prong power cord. The recalled Sauna Heater Kit is intended to attach to a customer-built wood frame.
Context & Analysis
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
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. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.
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