5 results
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11ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Open, Classified
×
Kidney Test
FDA Recall
Open, Classified
·GET TESTED INTERNATIONAL AB 59334 Vastervik Lysingsvagen 18 Vastervik Sweden·Product code QWZ·November 3, 2025
Liver Test
FDA Recall
Open, Classified
·GET TESTED INTERNATIONAL AB 59334 Vastervik Lysingsvagen 18 Vastervik Sweden·Product code QWZ·November 3, 2025
Allergy & Food Intolerance Test
FDA Recall
Open, Classified
·GET TESTED INTERNATIONAL AB 59334 Vastervik Lysingsvagen 18 Vastervik Sweden·Product code QWZ·November 3, 2025
EQ-400-RH-QZ and EQ-400-LH-BK products Product Usage: The device is a very broadband light source emitting incoherent non-laser light from the Deep UV through the visible wavelengths.
FDA Recall
Open, Classified
·Energetiq Technology Inc·Product code REK·September 27, 2019
STERIS Boot Assembly, Traction Device, OT 1000, Part Number REF 10009192
FDA Recall
Open, Classified
·Baxter Healthcare Corporation·Product code FWZ·February 14, 2024