WhichRecall
Class IIReported 2026-01-21

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

Recalled by Encon Safety Products Co

Reason for Recall

cGMP deviations.

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Recall Number
D-0260-2026
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2026-01-06
Reported
2026-01-21
Distribution
Nationwide within the United States
Code Info
Lot #: 239066, Exp. Date 1/24/2027; 378106, Exp. Date 3/8/2026; 379202, Exp. Date 3/29/2026; 379750, Exp. Date 4/24/2026; 380983, Exp. Date 5/24/2026; 382901, Exp. Date 7/11/2026; 384682, Exp. Date 8/16/2026; 386189, Exp. Date 9/20/2026; 387559, Exp. Date 10/11/2026; 388381, Exp. Date 11/2/2026; 398066, Exp. Date 1/24/2027; 389477, Exp. Date 2/21/2027; 392491, Exp. Date 3/13/2027; 393724, Exp. Date 4/3/2027, 394683, Exp. Date 4/29/2027; 395094, Exp. Date 5/29/2027; 395231, Exp. Date 6/18/2027; 395368, Exp. Date 7/17/2027, 397971, Exp. Date 11/8/2027; 398930, Exp. Date 8/28/2027; 399204, Exp. Date 9/25/2027; 400300, Exp. Date 10/16/2027; 403177, Exp. Date 11/8/2027; 403314, Exp. Date 11/25/2027; 405095, Exp. Date 1/24/2028; 406328, Exp. Date 2/14/2028; 407700, Exp. Date 4/3/2028; 407974, Exp. Date 4/17/2028; ; 410166, Exp. Date 6/13/2028; 410988, Exp. Date 7/1/2028.
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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