Data Foundry

Drug recalls 2026

Isotretinoin Capsules — Class II drug recall D-0446-2026

Ongoing recall by Teva Pharmaceuticals USA, Inc, reported 2026-04-15, distributed in FL, MS, OH, PR. Superpotent and Subpotent

Recall numberD-0446-2026
Product typeDrug
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmTeva Pharmaceuticals USA, Inc, Parsippany, NJ, United States
Recall initiated2026-01-12
Classified2026-04-08
Reported by FDA2026-04-15
DistributedFL, MS, OH, PR
Quantity8,376 packages
Reason classespotency
NDC00591-2433, 00591-2433-15, 00591-2433-45, 00591-2434, 00591-2434-15, 00591-2434-45, 00591-2435, 00591-2435-15, 00591-2435-45, 00591-2436, 00591-2436-15, 00591-2436-45, 00591-2451, 00591-2451-15, 00591-2451-45, 00591-2501, 00591-2501-15, 00591-2501-45
Lot numbers100075305, 100075512, 100076103
Expiration dates2027-06, 2027-07

Product

Isotretinoin Capsules, USP, 40 mg, 10 count Prescription Pacs, Rx only, Manufactured for: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, NDC 0591-2436-15 (carton), NDC 0591-2436-45 (blister pack).

Reason for recall

Superpotent and Subpotent

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-0446-2026. 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.