Data Foundry

Drug recalls 2026

ACETYLCYSTEINE SOLUTION — Class II drug recall D-0796-2026

Ongoing recall by American Regent, Inc., reported 2026-08-26, distributed nationwide. Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or

Recall numberD-0796-2026
Product typeDrug
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmAmerican Regent, Inc., Shirley, NY, United States
Recall initiated2026-07-24
Classified2026-08-26
Reported by FDA2026-08-26
DistributedNationwide (US)
Quantity316,450 vials
Reason classesforeign material, specification failure
NDC00517-7504, 00517-7504-01, 00517-7504-25, 00517-7510, 00517-7510-03, 00517-7604, 00517-7604-25, 00517-7610, 00517-7610-03, 00517-7630, 00517-7630-03
Lot numbers24418, 25131, 25349
Expiration dates2026-11-30, 2027-03-31, 2027-08-31

Product

ACETYLCYSTEINE SOLUTION, USP, 10% (100 mg/mL), packaged in a) 4 mL Vial NOT FOR INJECTION (NDC 0517-7504-01), and b) 25x4 mL Vials NOT FOR INJECTION (NDC 0517-7504-25), Rx Only, AMERICAN REGENT, INC., SHIRLEY, NY 11967.

Reason for recall

Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

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-0796-2026. 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.