Warning
Encon Safety Products Co Recalls AQ 120 GFEW
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Source: FDA
WarningRecall #D-0260-2026Drug / Pharmaceutical
Encon Safety Products Co Recalls AQ 120 GFEW
Encon Safety Products Co · Class II — Moderate Risk
Product Description
AQ 120 GFEW, Aquarion Preserved Cartridges (2) 3.7 Gallons each
Reason for Recall
cGMP deviations.
FDA Classification
Class II — Moderate Risk
A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution
Nationwide within the United States
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
The FDA classified this recall as Class II, indicating the pharmaceutical product may cause temporary health problems or poses a slight threat of a serious nature. Encon Safety Products Co initiated the recall on January 6, 2026 affecting 7677 bags. cGMP deviations. The product was distributed nationwide. Consumers should check their purchases and discontinue use of any affected product. Contact Encon Safety Products Co for further instructions.
Sources: FDA openFDA Enforcement Database
This recall appears in: Drug & Medication Defects.