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Class II: temporary or reversible health riskOngoing

Encon Safety Products Aq 120 Gfew Recall

AQ 120 GFEW, Aquarion Preserved Cartridges (2) 3

Encon Safety Products Co · Houston, TX

Risk level
Class II
Reported by FDA
Jan 21, 2026
Recall ID
D-0260-2026
Check your lot numberHow we source this data

Summary

Encon Safety Products recalled Aq 120 Gfew starting Jan 6, 2026. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0260-2026 on Jan 21, 2026. Reason: cGMP deviations. Status: Ongoing.

Why it was recalled

cGMP deviations.

Product description

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

Lot numbers, UPCs & expiration codes

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.

Where it was sold

Nationwide within the United States

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0260-2026
Classification
Class II
Status
Ongoing
Recall initiated
Jan 6, 2026
FDA report date
Jan 21, 2026
Quantity
7677 bags
Recall type
Voluntary: Firm initiated
Recalling firm
Encon Safety Products Co

Original FDA data

Every field from FDA enforcement report D-0260-2026, exactly as published.

Show all FDA fields
City
Houston
State
TX
Status
Ongoing
Country
United States
Event ID
98262
Address
6825 W Sam Houston Pkwy N
Code information
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.
Postal code
77041-4026
Report date
Jan 21, 2026
Product type
Drugs
Recall number
D-0260-2026
Classification
Class II
Recalling firm
Encon Safety Products Co
Product quantity
7677 bags
Reason for recall
cGMP deviations.
Voluntary / mandated
Voluntary: Firm initiated
Product description
AQ 120 GFEW, Aquarion Preserved Cartridges (2) 3.7 Gallons each
Distribution pattern
Nationwide within the United States
Recall initiation date
Jan 6, 2026
Initial firm notification
Letter
Center classification date
Jan 14, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0260-2026, published Jan 21, 2026. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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