RecallHawk

Tylö Halmstad and Kiruna Hybrid Saunas

Unknown Manufacturer

Summary

CPSC recalled Tylö Halmstad and Kiruna Hybrid Saunas by Unknown Manufacturer. Hazard: The saunas contain a bench that can collapse, posing a fall hazard to consumers.. Remedy: Consumers should stop using the Tylö Halmstad and Kiruna Hybrid Sauna benches immediately and contact Sauna360 for a free repair. Sauna360 will provide a professional installer to retrofit the benches with additional hardware. Consumers will also receive a revised product manual from Sauna360 that includes the weight limit..

Details

Source

cpsc

External ID

26040

Action Date

2025-10-23

Status

Ongoing

Category

product

Product Description

This recall involves bench seating in Sauna360's Tylö branded Halmstad and Kiruna Hybrid sauna rooms. The serial number for each room can be found on both the packaging and the sauna rooms. The Halmstad 2, 3, and 4 sauna rooms have the serial number label located beneath the upper bench on the left side, directly above the electrical contactor box. The Kiruna Hybrid 2 and 3 rooms have the serial number label applied to the right wall, located beneath the right side of the upper bench. The model number is printed in the manual. The following models and serial numbers are included in this recall: Recalled Model Numbers Range of Recalled Serial Numbers TRAD, Tylö Halmstad™ 2, W/BLISS, 15A, 120V, CB21-1, V1 CSFxxABTRxx-V1-4933 through CSFxxABTRxx-V1-6970 TRAD, Tylö Halmstad™ 2, W/BLISS, 20A, 120V, CB21-1, V1 TRAD, Tylö Halmstad™ 3, W/BLISS, 240V, CB23-1, V1 TRAD, Tylö Halmstad™ 4, W/BLISS, 240V, CB23-1, V1 IS, Tylö Kiruna Hybrid™ 2, W/BLISS, 15A, 120V, LOW EMR, CB20-1, V1 CSFxxABISxxTL-V1-4964 through CSFxxABISxxTL-V1-7224 IS, Tylö Kiruna Hybrid™ 2, W/BLISS, 20A, 120V, LOW EMR, CB20-1, V1 IS, Tylö Kiruna Hybrid™ 3, W/BLISS, 240V, LOW EMR, CB22-1, V1

Context & Analysis

Unknown Manufacturer has 1320 FDA actions in our database.

Frequently Asked Questions

How often does Unknown Manufacturer have FDA actions?

Unknown Manufacturer has 1320 FDA actions in our database, including 0 recalls and 0 device clearances.

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