Data Foundry

Drug recalls 2026

AQ 120 GFEW — Class II drug recall D-0260-2026

Ongoing recall by Encon Safety Products Co, reported 2026-01-21, distributed nationwide. cGMP deviations.

Recall numberD-0260-2026
Product typeDrug
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmEncon Safety Products Co, Houston, TX, United States
Recall initiated2026-01-06
Classified2026-01-14
Reported by FDA2026-01-21
DistributedNationwide (US)
Quantity7,677 bags
Reason classescgmp
Lot numbers239066, 378106, 379202, 379750, 380983, 382901, 384682, 386189, 387559, 388381, 389477, 392491, 393724, 394683, 395094, 395231, 395368, 397971, 398066, 398930, 399204, 400300, 403177, 403314, 405095, 406328, 407700, 407974, 410166, 410988
Expiration dates2026-03-08, 2026-03-29, 2026-04-24, 2026-05-24, 2026-07-11, 2026-08-16, 2026-09-20, 2026-10-11, 2026-11-02, 2027-01-24, 2027-02-21, 2027-03-13, 2027-04-03, 2027-04-29, 2027-05-29, 2027-06-18, 2027-07-17, 2027-08-28, 2027-09-25, 2027-10-16, 2027-11-08, 2027-11-25, 2028-01-24, 2028-02-14, 2028-04-03 and 3 more

Product

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

Reason for recall

cGMP deviations.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0260-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.