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Adverse-event reports (MAUDE)

Read this first: MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line shows reporting volume for the average device in the same FDA product code — a reporting baseline, not a risk measure.

No adverse-event reports are linked to this device.

Recall history

No recalls linked.

Regulatory clearances

None linked.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2024-12-06WLWarning LetterRandox Laboratories Limited
2024-12-06WLWarning LetterRandox Laboratories Limited
2024-08-08OAIOfficial action indicatedRandox Laboratories Limited0
2024-08-08OAIOfficial action indicatedRandox Laboratories Limited0
2016-04-28VAIVoluntary action indicatedRandox Laboratories, Limited1
2016-04-28VAIVoluntary action indicatedRandox Laboratories, Limited1
2016-04-28VAIVoluntary action indicatedRandox Laboratories, Limited1
2016-04-28VAIVoluntary action indicatedRandox Laboratories, Limited1
2016-04-28VAIVoluntary action indicatedRandox Laboratories, Limited1
2016-04-28VAIVoluntary action indicatedRANDOX LABORATORIES, LTD.1
2013-12-05VAIVoluntary action indicatedRANDOX TEORANTA2
2012-11-29VAIVoluntary action indicatedRandox Laboratories, Limited5
2012-11-29VAIVoluntary action indicatedRandox Laboratories, Limited5
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