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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Topical Products

Aquarion Preserved Cartridges Recalled for cGMP Quality Violations

Agency Publication Date: January 14, 2026
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Summary

Encon Safety Products Co. is recalling approximately 7,677 bags of Aquarion Preserved Cartridges (AQ 120 GFEW), which are used in emergency eyewash stations. The recall was initiated due to deviations from Current Good Manufacturing Practice (cGMP) requirements, which are standards that ensure products are made safely and correctly. Each package contains two 3.7-gallon cartridges with various lot numbers and expiration dates ranging from 2026 to 2028. If you have these products, you should contact the manufacturer or your distributor to arrange for their return.

Risk

The failure to follow required manufacturing practices can lead to products that are not sterile or do not meet quality specifications. In an emergency eyewash situation, using a product with quality deviations could potentially lead to infection or further eye irritation rather than providing safe relief.

What You Should Do

  1. Identify if you have the recalled AQ 120 GFEW Aquarion Preserved Cartridges by checking the lot number and expiration date printed on the bags.
  2. Check for the following lot numbers: 239066, 378106, 379202, 379750, 380983, 382901, 384682, 386189, 387559, 388381, 398066, 389477, 392491, 393724, 394683, 395094, 395231, 395368, 397971, 398930, 399204, 400300, 403177, 403314, 405095, 406328, 407700, 407974, 410166, or 410988. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled product immediately and remove it from any emergency eyewash stations.
  4. Contact Encon Safety Products Co. or your authorized distributor to arrange for the return of the affected cartridges.
  5. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional assistance or to report any adverse events.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return.

Affected Products

Product: AQ 120 GFEW, Aquarion Preserved Cartridges (3.7 Gallons)
Variants: 2 cartridges per bag
Model:
AQ 120 GFEW
Lot Numbers:
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)

Recall #: D-0260-2026

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98262
Status: Active
Manufacturer: Encon Safety Products Co
Sold By: Authorized distributors; Safety equipment retailers
Manufactured In: United States
Units Affected: 7677 bags
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.