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
| Initiated | Recall # | Class | Status | Reason | Quantity | Link basis |
|---|---|---|---|---|---|---|
| 2018-03-20 | Z-1353-2018 | Class II | Terminated | Firm 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, NY | 748 units | clearance family |
Regulatory clearances
None linked.
Manufacturer compliance record
| Date | Type | Outcome | Facility | Citations |
|---|---|---|---|---|
| 2025-05-15 | VAI | Voluntary action indicated | Certified Safety Manufacturing, Inc. | 1 |
| 2019-10-15 | VAI | Voluntary action indicated | Certified Safety Manufacturing, Inc. | 7 |
| 2013-08-29 | VAI | Voluntary action indicated | Certified Safety Manufacturing, Inc. | 3 |
| 2010-01-13 | NAI | No action indicated | Certified Safety Manufacturing, Inc. | 0 |
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