THOR Photomedicine Ltd recalls NovoTHOR Whole Body Light Pod, Gen 3.0 (1) Product Code S2188 - Reg (2) Product Code S2189 - Reg PRX (3) Product Code S2190 - XL
One of the ball studs attaching a gas strut to the canopy may fail. There is potential risk of injury should a ball stud fail when someone is in the NovoTHOR and trying to open or close the canopy
Read the official notice →- Date
- 2024-02-07
- Country
- United States
- Brand
- THOR Photomedicine
- Product
- NovoTHOR Whole Body Light Pod, Gen 3.0 (1) Product Code S2188 - Reg (2) Product Code S2189 - Reg PRX (3) Product Code S2190 - XL
- Classification
- Class II
- Units
- Domestic distribution to the states of Arizona California Colorado Connecticut…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More THOR Photomedicine recalls
- 2025-09-03
USTHOR Photomedicine Ltd recalls Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Model/Catalog Number: S2186 Software Version: N/A Product Description: The…
The potential for a failed welded nut to shear off. When this occurs, the gas strut on one side of the device becomes detached from the canopy, making the canopy difficult to lift.
FDA · DeviceTHOR Photomedicine LtdWorldwide distribution: US (nationwide): AK, AZ, CA, CO, CT, FL, GA, HI, ID,…Official notice →- 2023-12-13
- US
Thor Photomedicine Ltd recalls NovoTHOR Gen 2.5 Regular whole body red light therapy bed, model S2183
Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift.
FDA · DeviceThor Photomedicine LtdWorldwide Distribution: US (Nationwide): Arizona, California, Colorado,…Official notice →
Other drugs & medical recalls in the United States
- 2024-02-14
- US
- US
- US
- 2024-02-07
- US
Draegerwerk Ag & Co. Kgaa recalls Atlan, Gas Machine for Anesthesia or Analgesia, Catalog numbers 8621500 (Atlan A350) and 8621600 (Atlan A350 XL)
Internal backup battery may fail spontaneously while the Atlan is being operated without AC mains supply, resulting in unexpected shutdown of the device while running on batteries.
FDA · DeviceDraegerwerk Ag & Co. KgaaNo devices were distributed to end-users (customers) in the US. All devices…Official notice → - US
Vortex Surgical Inc. recalls Vortex Surgical ACTU8 FORCEPS, 25 GA, ADAPTIVE, REF VS0740.25
Reason for the voluntary recall is residue was identified on the two forceps tips of a customer in Korea. The residue is associated with one lot of forceps tips which were utilized in two lots of ACTU8 Adaptive Forceps…
FDA · DeviceVortex Surgical Inc.Worldwide - US Nationwide distribution in the states of OH, WA, MN, MI, IA and…Official notice → - US
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE BLOOD CULTURE KIT, Reorder Number DYNDH1723
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not…