Recalls / Class II

Class IID-0260-2026

Product

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

Affected lot / 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.

Why it was recalled

cGMP deviations.

Recalling firm

Firm

Encon Safety Products Co

Notification channel

Letter

Type

Voluntary: Firm initiated

Address

6825 W Sam Houston Pkwy N, Houston, Texas 77041-4026

Distribution

Quantity

7677 bags

Distribution pattern

Nationwide within the United States

Timeline

Recall initiated

2026-01-06

FDA classified

2026-01-14

Posted by FDA

2026-01-21

Status

Ongoing

Source: openFDA Drug Enforcement endpoint. Recall record D-0260-2026. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.