Chiesi Usa, Inc. — Cleviprex recall — Check your batch

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Chiesi Usa, 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 2026-07-22

Lack of Assurance of Sterility

CLEVIPREX (clevidipine injectable emulsion) 50 mg/100 mL (0.5 mg/mL), 10 Single Use Vials, Rx Only, Manufactured for: Chiesi USA, Inc., Cary, NC 27518, by Fresenius Kabi, Graz, Austria, NDC 10122-611-10.

Check these codes: Lot #: 1239521, 1237454, Exp. Date 10/2027

44280 vials · distributed nationwide within the united states Recall D-0689-2026 on FDA.gov ↗

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