PlainRecalls

Thor Photomedicine Ltd

Compiled from official public sources by the publisher.

9 recalls on record · Latest: Sep 3, 2025

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Agency notice ledger

Federal filing book Thor Photomedicine Ltd LIGHT-BOOK · SINGLE-AGENCY

#1,676 of 14,151 · 9 notices · 0.009% archive

  • BOOK 9 notices
  • RANK #1,676 of 14,151
  • SHARE 0.009% archive
  • AGENCY FDA Devices (9)
  • CAT medical devices
  • CATS 1 category
  • LATEST Sep 3, 2025
  • PHOTO 3Cs Organics LLC

Nearest notice-volume peer: 3Cs Organics LLC (0 notice gap)

Thor Photomedicine Ltd accounts for about 0.009% of the 104,423-notice archive on 9 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Where Thor Photomedicine Ltd sits among 14,151 recalling firms

Thor Photomedicine Ltd ranks 1,676th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Thor Photomedicine Ltd vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

9 1676th of 14151 higher than 12,464 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Thor Photomedicine Ltd in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Thor Photomedicine Ltd holds about 0.009% of archive notices alongside 9 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Sep 3, 2025

Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Model/Catalog Number: S2186 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 circulation, temporary relief of minor muscle and joint pain and stiffness, minor arthritis pain, muscle spasm, and temporary relaxation of muscles. Component: N/A
FDA Devices Moderate Sep 3, 2025

Brand Name: THOR Product Name: NovoTHOR XL Model/Catalog Number: S2190 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 circulation, temporary relief of minor muscle and joint pain and stiffness, minor arthritis pain, muscle spasm, and temporary relaxation of muscles. Component: No
FDA Devices Moderate Sep 3, 2025

Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Model/Catalog Number: S2189 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 circulation, temporary relief of minor muscle and joint pain and stiffness, minor arthritis pain, muscle spasm, and temporary relaxation of muscles. Component: N/A
FDA Devices Moderate Sep 3, 2025

Brand 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 circulation, temporary relief of minor muscle and joint pain and stiffness, minor arthritis pain, muscle spasm, and temporary relaxation of muscles. Component: No
FDA Devices Moderate Feb 7, 2024

NovoTHOR Whole Body Light Pod, Gen 3.0 (1) Product Code S2188 - Reg (2) Product Code S2189 - Reg PRX (3) Product Code S2190 - XL
FDA Devices Moderate Dec 13, 2023

NovoTHOR Gen 2.5 Regular whole body red light therapy bed, model S2183
FDA Devices Moderate Dec 13, 2023

NovoTHOR Gen 2.0 whole body red light therapy bed, model S1176
FDA Devices Moderate Dec 13, 2023

G041 POD, THOR NOVO GEN 2.0 XL whole body red light therapy bed, model S1177
FDA Devices Moderate Dec 13, 2023

NovoTHOR Gen 2.5 XL whole body red light therapy bed, model S2184.

Thor Photomedicine Ltd holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Frequently Asked Questions

How many federal recall notices name Thor Photomedicine Ltd? ▼
PlainRecalls indexes 9 distinct federal recall events naming Thor Photomedicine Ltd, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Thor Photomedicine Ltd sit among other recalling firms? ▼
Thor Photomedicine Ltd ranks #1,676 of 14,151 by distinct recall-event count among 14,151 firms in this archive (88th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Thor Photomedicine Ltd's notices? ▼
FDA Devices accounts for 9 of this firm's 9 indexed notices.
What product category dominates Thor Photomedicine Ltd's filing book? ▼
Filings for Thor Photomedicine Ltd span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Thor Photomedicine Ltd: 9 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Thor Photomedicine Ltd; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026