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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
InitiatedRecall #ClassStatusReasonQuantityLink basis
2018-03-20Z-1353-2018Class IITerminatedFirm is recalling first aid/emergency kits and cabinets which contain Honeywell Eyewash (3 lots) which is being recalled due to leaking bottles.Distribution: US Nationwide Distribution in the states of NE, KY, CA, OH, TX, NC, AL, NJ, TN, MN, IA, MO, MA, MI, ME, BY, GA, WA, LA, IL, VA, NY748 unitsclearance family
Regulatory clearances

None linked.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2025-05-15VAIVoluntary action indicatedCertified Safety Manufacturing, Inc.1
2019-10-15VAIVoluntary action indicatedCertified Safety Manufacturing, Inc.7
2013-08-29VAIVoluntary action indicatedCertified Safety Manufacturing, Inc.3
2010-01-13NAINo action indicatedCertified Safety Manufacturing, Inc.0
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