Recall Register

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THOR Photomedicine Ltd

FDA recalling firm · 3 enforcement events · 9 product records · 2022–2025

THOR Photomedicine Ltd has 3 FDA enforcement events on this register (9 product records) between 2022 and 2025: 3 device; the busiest year was 2022 with 1.

0% of its events are Class I; the most common class is Class II (3). 3 events are listed as ongoing.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

InitiatedProduct (first record)TypeClassRecordsStatus
24 Jul 2025Brand Name: THOR Product Name: NovoTHOR Model/Catalog Number: S2188 Software Version: N/A Product Description: The NovoTHOR and NovoTHOR XL are intended to emit energy in the visible and IR spectrum to provide topical heating for the purpose of elevating tissue temperature for temporary increase in local blood…DeviceClass II4Ongoing
20 Nov 2023NovoTHOR Whole Body Light Pod, Gen 3.0 (1) Product Code S2188 - Reg (2) Product Code S2189 - Reg PRX (3) Product Code S2190 - XLDeviceClass II1Ongoing
13 Sep 2022NovoTHOR Gen 2.0 whole body red light therapy bed, model S1176DeviceClass II4Ongoing

By type and class

Device3
Class II3

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

22
23
24
25
26
Enforcement events for THOR Photomedicine Ltd by year initiated.

Questions and answers

How many FDA recalls has THOR Photomedicine Ltd had?

3 enforcement events (9 product records) on this register, 2022–2025: 3 device.

Are any THOR Photomedicine Ltd recalls ongoing?

3 events are listed as ongoing in the current openFDA export.

What class are THOR Photomedicine Ltd recalls?

3 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.