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Recall Observatory FDA recall evidence

Drug product

Lisdexamfetamine Dimesylate Capsules, 70 mg, CII, 100-count bottle, Rx only, Manufactured by: OHM Laboratories, New Brunswick, NJ 08901, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 57664-052-88.

D-0150-2026

October 28, 2025

Class II

Product summary

Firm
SUN PHARMACEUTICAL INDUSTRIES INC
Event
Event 97874
Status
Ongoing
Classification
Class II
Quantity
N/A
Official record key
drug-enforcement:D-0150-2026

Official wording

Reason: Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 12-month long term stability station (25¿C, 60%RH) for Lisdexamfetamine dimesylate capsules.

Code information: Lot #: AD48712, Expiry: 4/30/2026; AD50898, Expiry: 5/31/2026.

Distribution pattern: U.S Nationwide.

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    out of specification