Encon Recalls Aquarion Preserved Cartridges Due to cGMP Deviations
Encon Safety Products recalls AQ 120 GFEW Aquarion cartridges due to current Good Manufacturing Practice deviations. Check lot numbers and expiration dates.
Recall notice
cGMP deviations.
Contact the company
What happened, in plain English
Encon Safety Products Co is recalling AQ 120 GFEW Aquarion Preserved Cartridges because of current Good Manufacturing Practice (cGMP) deviations. The recall affects 7,677 bags distributed nationwide within the United States. The specific nature of these manufacturing deviations and any resulting health risks are not detailed in the provided record. Read more at govinfonow.com/recall/31558-encon-recalls-aquarion-preserved-cartridges-due-to-cgmp-deviations.
Source Summary by GovInfoNow · govinfonow.com/recall/31558-encon-recalls-aquarion-preserved-cartridges-due-to-cgmp-deviations · Updated October 9, 2026 · FDA enforcement record: FDA #D-0260-2026
Cite this page
“Encon Recalls Aquarion Preserved Cartridges Due to cGMP Deviations.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/31558-encon-recalls-aquarion-preserved-cartridges-due-to-cgmp-deviations. Based on FDA recall #D-0260-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0260-2026%22&limit=1).
Why it’s dangerous
The recall is due to cGMP deviations, which means the product may not have been manufactured according to required quality standards. The record does not explain what specific defects occurred or how they could affect safety or efficacy.
Who’s affected
Consumers or facilities in the United States who purchased AQ 120 GFEW Aquarion Preserved Cartridges from Encon Safety Products Co. It is unclear who is most at risk because the record does not specify the nature of the cGMP deviations.
How to tell if you have this one
Check if you have AQ 120 GFEW Aquarion Preserved Cartridges (2) 3.7 Gallons each. Verify the lot number against this list: 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, 410988. Match the expiration date to the lot: 239066 (1/24/2027), 378106 (3/8/2026), 379202 (3/29/2026), 379750 (4/24/2026), 380983 (5/24/2026), 382901 (7/11/2026), 384682 (8/16/2026), 386189 (9/20/2026), 387559 (10/11/2026), 388381 (11/2/2026), 398066 (1/24/2027), 389477 (2/21/2027), 392491 (3/13/2027), 393724 (4/3/2027), 394683 (4/29/2027), 395094 (5/29/2027), 395231 (6/18/2027), 395368 (7/17/2027), 397971 (11/8/2027), 398930 (8/28/2027), 399204 (9/25/2027), 400300 (10/16/2027), 403177 (11/8/2027), 403314 (11/25/2027), 405095 (1/24/2028), 406328 (2/14/2028), 407700 (4/3/2028), 407974 (4/17/2028), 410166 (6/13/2028), 410988 (7/1/2028).
- Brand
Encon Safety Products- Category
Drug
What to do — step by step
Check your product details
Verify if you have the recalled AQ 120 GFEW Aquarion Preserved Cartridges by checking the lot number and expiration date.
Contact the manufacturer
The record does not specify a remedy or return process; contact Encon Safety Products Co for further instructions.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide within the United States” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 15 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0260-2026 (January 6, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0260-2026 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.