US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Jan 6, 2026 (8 months ago)

AQ 120 GFEW, Aquarion Preserved Cartridges (2) 3.7 Gallons each

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

cGMP deviations.

What was recalled

AQ 120 GFEW, Aquarion Preserved Cartridges (2) 3.7 Gallons each

Recalling firm
Encon Safety Products Co
Origin
TX, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0260-2026

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.