CW ClaimWatch Consumer alert tracker

Recall

ACCORD BIOPHARMA INC: IMULDOSA, (ustekinumab-srlf) Injection, 130 mg/26 mL (5mg/mL), Rx only, Single dose vial, Recall

Lack of assurance of Sterility: Product details: 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, Bloo...

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Agency
FDA
Record ID
D-0653-2026
Canonical
https://claimwatch-mvp.vercel.app/item/accord-biopharma-inc-imuldosa-ustekinumab-srlf-injection-130-mg-26-ml-5mg-ml-rx-only-singl/

What happened?

Lack of assurance of Sterility: Product details: 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, Bloo...

Who may be affected?

US Nationwide.

What should consumers do?

Affected quantity: 326 vials

Official source

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No. This page is informational. Always confirm eligibility, deadlines, and safety instructions through official sources.

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