FDA recall, , Moderate risk
Encon Safety Products Aquarion Preserved Cartridges
The Aquarion Preserved Cartridges have cGMP deviations.
Summary by Recall Canary from the FDA notice
What happened
Encon Safety Products Co, of Houston, Texas, recalled AQ 120 Gfew, Aquarion Preserved Cartridges (2) 3.7 Gallons each, due to cGMP deviations. The recall began on January 6, 2026, and was added to the FDA's Enforcement Report on January 14, 2026. The products were distributed nationwide within the United States.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is yours affected?
Affected if its lot code is listed.
AQ 120 Gfew, Aquarion Preserved Cartridges (2) 3.7 Gallons each
- Lot code
- 239066
- 378106
- 379202
- 379750
- 380983
- 382901
- 384682
- 386189
- 387559
- 388381
- 398066
- 389477
- 392491
- 393724
- 395094
- 395231
- 395368
- 398930
- 399204
- 400300
- 403177
- 403314
- 405095
- 406328
- 407700
- 407974
- 410988
Recall details
- Company began the recall
- Sold in
Nationwide within the United States
- Company
- Encon Safety Products CoHouston, Texas
- Hazard
- Manufacturing problem
- Risk
Moderate risk
Taking it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98262
- Recall number
- D-0260-2026
- Quantity recalled
- 7677 bags
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
Summary updated
