# FDA recall Z-1353-2018

> **Certified Safety Mfg Inc** · Class II · device recall initiated 2018-03-20.

## Product

First aid/emergency kits containing Honeywell eyewash:  CSM kit number	Kit/cabinet Description	CSM Eyewash#	 Size:	Honeywell Part#   K206125	LXXV - 75V " Economy Cabinet 3 Shelf	R508016	Eye Wash " 4 oz.	32-000452-0000  K 206154	LXXV - 75V " Deluxe Cabinet ¿3 Shelf 	RS08016	Eye Wash - 4 oz.	32-000452-0000  K206210	FAC- 3 ¿Deluxe Cabinet ¿3 Shelf 	R508016	Eye Wash - 4 oz.	32-000452-0000  K606999	ZLB¿CSX CPR Kit 37	R508016	Eye Wash " 4 oz.	32-000452-0000  KR206152	FAC " 4R ¿200 Person Deluxe Cabinet - Refill 	R508016	Eye Wash ¿4 oz.	32-000452-0000  K608054	Cement Burn Cabinet	R511018	Eye Wash " 16 oz. 	32-000454 0000- H5  K610045	FAC.3 " Deluxe Cabinet .w/BBP .NO MEDS .3 Shelf 	R508016	Eye Wash " 4 oz.	32-000452-0000  K606289	Eye Wash Cabinet ¿316	R511018	Eye Wash - 16oz	32-000454-0000-HS  K608061	36M¿Delmarva  Power/ACE¿w/Logo 	R508016	Eye Wash¿4 oz.	32-000452-0000  K611017	16PW " Hospeco " w/logo	R508016	Eye Wash " 4 oz.	32-000452-0000  K206152	FAC¿4 ¿200 Person Deluxe Cabinet ¿4 Shelf 

## Reason for recall

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

## Key facts

- **Recall number:** Z-1353-2018
- **Recalling firm:** Certified Safety Mfg Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-03-20
- **Report date:** 2018-04-18
- **Termination date:** 2020-09-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Kansas City, MO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1353-2018

## Citation

> AI Analytics. FDA recall Z-1353-2018. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-1353-2018. Source: US FDA. Licensed CC0.

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