WhichRecall
Class IIReported 2025-02-05

Inflectra (infliximab-dyyb), For injection, 100mg per vial, packaged in 10 mL single-dose vial, Rx only, Mfd by: CELLTRION, INC, Dist. by: Pfizer Labs, Division of Pfizer Inc., New York, NY 10001, NDC 0069-0809-01

Recalled by McKesson

Reason for Recall

cGMP Deviations: Product intended for quarantine was inadvertently distributed.

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Recall Number
D-0213-2025
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2025-01-17
Reported
2025-02-05
Distribution
Nationwide USA
Code Info
Lot# 04647349, Exp Date 5/31/2029
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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