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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
2018-08-17NAINo action indicatedBayer Medical Care, Inc.0
2018-08-17NAINo action indicatedBayer Medical Care, Inc.0
2017-01-19NAINo action indicatedBayer Medical Care, Inc.0
2017-01-19NAINo action indicatedBayer Medical Care, Inc.0
2017-01-18NAINo action indicatedBayer Medical Care, Inc.0
2017-01-18NAINo action indicatedBayer Medical Care, Inc.0
2017-01-06NAINo action indicatedBayer Medical Care, Inc.0
2017-01-06NAINo action indicatedBayer Medical Care, Inc.0
2015-04-16NAINo action indicatedBayer Medical SRL0
2014-03-20NAINo action indicatedBayer Medical Care Inc.0
2013-08-12NAINo action indicatedBayer Medical Care, Inc.0
2013-08-12NAINo action indicatedBayer Medical Care, Inc.0
2013-08-07NAINo action indicatedBayer Medical Care, Inc.0
2013-08-07NAINo action indicatedBayer Medical Care, Inc.0
2013-08-01NAINo action indicatedBayer Medical Care, Inc.0
2013-08-01NAINo action indicatedBayer Medical Care, Inc.0
2012-05-02NAINo action indicatedBayer Medical Care, Inc.0
2012-05-02NAINo action indicatedBayer Medical Care, Inc.0
2011-08-23NAINo action indicatedBayer Medical Care, Inc.0
2011-08-23NAINo action indicatedBayer Medical Care, Inc.0
2011-05-19WLWarning LetterBayer Medical Care, Inc.
2011-05-19WLWarning LetterBayer Medical Care, Inc.
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