Accord Biopharma INC — Imuldosa recall — Check your batch

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Accord Biopharma INC

Check your batch

Check the batch codes below. If yours matches, return it for a refund rather than take it.

Class II

May cause temporary or medically reversible harm. Serious consequences are unlikely.
Refunds don't require a receipt, and you don't need proof of purchase.
FDA status: Ongoing.

What was recalled

Source: FDA · synced 29 Jul 2026 13:14

Check your batch Filed 2026-07-08

Lack of assurance of Sterility:

IMULDOSA, (ustekinumab-srlf) Injection, 130 mg/26 mL (5mg/mL), Rx only, Single dose vial, Manufactured by Accord BioPharma Inc., 8041 Arco corporate Drive, Suite 200, Raleigh, NC 27617, USA, Manufactured at: Catalent Indiana, LLC, 1300 S. Patterson Drive, Bloomington, IN 47403, USA, NDC 69448-019-26.

Check these codes: Lot # 004L24A, Exp Date: 02/19/2027.

326 vials · distributed us nationwide. Recall D-0653-2026 on FDA.gov ↗

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