URGENT: DRUG RECALL- AQ120 GFEW, AQUARION PRESERVED CARTRIDGES (2) @ 3.7 GALLON EACH

URGENT: DRUG RECALL- AQ120 GFEW, AQUARION PRESERVED CARTRIDGES (2) @ 3.7 GALLON EACH

Dear Industrial Consumers and Distributors:

This is to inform you of a product recall involving:

AQUARION REFILL CARTRIDGE AQ120 PRESERVED CARTRIDGES (2) @ 3.7 GALLONS EACH

This voluntary recall has been initiated due to inadequate current good manufacturing practice
requirements for AQ120 Non-Sterile Eyewash Cartridges. Use of this product could result in a range
of ocular infections such as bacterial keratitis or endophthalmitis. Immunocompromised individuals,
those sustaining ocular injuries that damage the corneal epithelium, and those sustaining penetrating
ocular injuries are at higher risk of potential infection. To date, Encon Safety Products has not received
any reports of adverse events related to this voluntary recall.

We began shipping this product on December 2023 through November 2025 in the USA consisting of
7,677 units.

Immediately examine your inventory and quarantine product subject to recall. In addition, if you may have
further distributed this product, please identify your customers and notify them at once of this product recall.
Your notification to your customers may be enhanced by including a copy of this recall notification letter.

For product that is recalled, please provide the following on the enclosed form:

• Lot Number:
• Date of Destruction:
• Witness of product destruction (name and company)
• Photo of destroyed bag including lot number and expiry date
• Location of destruction

Please complete and return the enclosed response form as soon as possible via email or hard copy.

productsafety@enconsafey.com

This voluntary recall is being made with the knowledge of the Food and Drug Administration.

If you have any questions, please call 800-283-6266.

Sincerely,

Additional Recall Documents and Product Images

Read the Official Notice:

AQ120 Voluntary Recall Notice (PDF)

Access the Destruction Verification form:

Recall Destruction Verification Form (DOCX)