18 results
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21ms
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Sources: EU EUDAMED, US FDA
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Status: Open, Classified
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The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.
FDA Recall
Open, Classified
·IN MY BATHROOM LLC·Product code RHP·January 27, 2022
The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range with an intended use of disinfecting surfaces.
FDA Recall
Open, Classified
·MAX LUX CORP 03e 01 01 Yangxi Indust Ry Zone Yangjiangyangjiang China·Product code RHP·October 26, 2021
The product is a handheld ultraviolet-C germicidal wand and contains narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.
FDA Recall
Open, Classified
·PHONESOAP·Product code RHP·August 30, 2022
The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emission wavelength at 254 nm.
FDA Recall
Open, Classified
·Uvlizer c/o RAIS INTERNATIONAL LLC·Product code RHP·March 6, 2026
The product is a handheld ultraviolet-C germicidal wand and contains a narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.
FDA Recall
Open, Classified
·BigTree Sales Inc.·Product code RHP·August 29, 2025
The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.
FDA Recall
Open, Classified
·MERCHSOURCE LLC·Product code RHP·August 1, 2022
The product is a handheld ultraviolet-C germicidal wand and contains a combination of five UV-A and UV-C LED lights. The product comes in two configurations: UV-C x 1; UV-A x 4, or UV-C x 2; UV-A x 3. The product has two peak emission wavelengths at 274 nm and 397 nm.
FDA Recall
Open, Classified
·Uvlizer c/o RAIS INTERNATIONAL LLC·Product code RHP·March 6, 2026
OttLite Rechargeable UVC Disinfecting Wand
FDA Recall
Open, Classified
·Ottlite TEchnologies, Inc.·Product code RHP·November 17, 2022
VITROS Chemistry Products LAC Slides. Catalog Number: 8150112. 1 Sales Unit = contains 5 cartridges of 18 slides, for a total of 90 tests.
FDA Recall
Open, Classified
·Ortho-Clinical Diagnostics, Inc.·Product code KHP·July 29, 2025
Atellica IM Enhanced Estradiol (eE2) (REF) 500T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 11206250 All lots
FDA Recall
Open, Classified
·Siemens Healthcare Diagnostics, Inc.·Product code CHP·March 3, 2022
Atellica IM Enhanced Estradiol (eE2) 100T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10995561 All lots
FDA Recall
Open, Classified
·Siemens Healthcare Diagnostics, Inc.·Product code CHP·March 3, 2022
VIDAS CLINICAL VIDAS ESTRADIOL II 60 TESTS, CATALOG 30431-01
FDA Recall
Open, Classified
·Biomerieux Inc·Product code CHP·November 9, 2022
VIDAS Estradiol II, REF 30431-01
FDA Recall
Open, Classified
·bioMerieux, Inc.·Product code CHP·September 22, 2021
Atellica IM Enhanced Estradiol (eE2) 500T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10995562 All lots
FDA Recall
Open, Classified
·Siemens Healthcare Diagnostics, Inc.·Product code CHP·March 3, 2022
ADVIA Centaur Enhanced Estradiol (eE2) 100T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10490889 All lots
FDA Recall
Open, Classified
·Siemens Healthcare Diagnostics, Inc.·Product code CHP·March 3, 2022
ADVIA Centaur Enhanced Estradiol (eE2) 500T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10491445 All lots
FDA Recall
Open, Classified
·Siemens Healthcare Diagnostics, Inc.·Product code CHP·March 3, 2022
ADVIA Centaur Enhanced Estradiol (eE2) (REF) 500T - In vitro diagnostic use in the quantitative detection of estradiol SMN: 10697757 All lots
FDA Recall
Open, Classified
·Siemens Healthcare Diagnostics, Inc.·Product code CHP·March 3, 2022
Chemistry Products LAC Slides. Catalog Number: 8433880. 1 Sales Unit = contains 5 cartridges of 60 slides, for a total of 300 tests.
FDA Recall
Open, Classified
·Ortho-Clinical Diagnostics, Inc.·Product code KHP·July 29, 2025