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Thor Photomedicine Ltd Watermeadow House Chesham United Kingdom

Thor Photomedicine Ltd Watermeadow House Chesham United Kingdom Recalls

All product recalls associated with Thor Photomedicine Ltd Watermeadow House Chesham United Kingdom.

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Recall Summary

Total Recalls

1000

Past Year

276

Class I (Serious)

242

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1101–1120 of 4099 recalls

NOVO GEN 2.0 XL Bed (Thor) – Gas Strut Detachment (2022)

Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift.

FDASep 13, 2022Nationwide• Thor Photomedicine Ltd Watermeadow House Chesham United Kingdom

NovoTHOR Gen 2.0 (Thor) – Gas Strut Detachment (2022)

Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift.

FDASep 13, 2022Nationwide• Thor Photomedicine Ltd Watermeadow House Chesham United Kingdom

NovoTHOR Gen 2.5 XL (Thor) – Gas Strut Detachment (2022)

Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift.

FDA

1...54 555657 58...205

Page 56 of 205Next

Sep 13, 2022

Nationwide

• Thor Photomedicine Ltd Watermeadow House Chesham United Kingdom

RS Helmet (BatteryJack) – Impact Protection Failure (2022)

BatteryJack Inc. (BatteryJack) is recalling certain RS helmets, model TN-0700, sizes SM, MED, LRG, and XL. The helmets may not adequately protect the wearer in the event of a head impact during a crash. As such, these helmets fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 218, "Motorcycle Helmets."

NHTSAAug 17, 2022Nationwide• BATTERYJACK

Olympus PowerSeal 5MM Sealer (Olympus) – Rotation Knob Issue (2022)

An out of specification component preventing the blue retention ring from keeping the rotation knob in place. This may result in a loose rotation collar and retention ring and cause delay of treatment

FDAAug 12, 2022Nationwide• Olympus Corporation of the Americas

Olympus PowerSeal 5MM Sealer (Olympus) – Rotation Knob Issue (2022)

FDAAug 12, 2022Nationwide• Olympus Corporation of the Americas

Olympus PowerSeal 5MM Sealer (Olympus) – Rotation Knob Issue (2022)

FDAAug 12, 2022Nationwide• Olympus Corporation of the Americas

Home Elevators (Residential Elevators) – entrapment risk (2022)

This recall involves Residential Elevators, Inc. residential elevator models Easy Rider, Horizon Lift, Luxury Lift, Luxury Lift Hydraulic, Luxury Lift Traction and RE. The Residential Elevators brand name is printed on the light in the operating panel inside the elevator cab. The elevators are used in consumers' homes.

CPSCAug 11, 2022Nationwide• Residential Elevators, Inc., of Tallahassee, Fla.

Verify SixCess Challenge Pack (Steris) – Chemical Indicator Error (2022)

Product contains incorrect chemical indicators in packaging.

FDAAug 10, 2022AK, AZ, AR +28 more• Steris Corporation Hopkins Facility

MEGA Intra-Aortic Balloon (Datascope) – Dilator Size (2022)

Certain lots containing undersized dilator.

FDAAug 5, 2022Nationwide• Datascope Corporation

Sensation Insertion Kit (Datascope) – Dilator Size (2022)

Certain lots containing undersized dilator.

FDAAug 5, 2022Nationwide• Datascope Corporation

LINEAR IAB (Datascope) – Volume Labeling (2022)

The balloon volume is incorrectly described as 34cc instead of 40cc on one of the three internal labels enclosed for hospital use. A labelling error may result in user confusion and/or delay in initiating therapy. Therapy delays may impact those patients who are more hemodynamically unstable.

FDAAug 5, 2022Nationwide• Datascope Corporation

Sensation Plus IAB (Datascope) – Dilator Size (2022)

Certain lots containing undersized dilator.

FDAAug 5, 2022Nationwide• Datascope Corporation