US Drug Recall Register
Class I · High risk Terminated Initiated May 11, 2019 (7 years ago)

Promacta (eltrombopag) 12.5 mg for Oral Suspension, Rx Only Manufactured by: Halo…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Cross Contamination with Other Products: product is being recalled due to possible cross-contamination with peanut flour.

What was recalled

Promacta (eltrombopag) 12.5 mg for Oral Suspension, Rx Only Manufactured by: Halo Pharmaceuticals, Inc. Whippany, New Jersey 07981 Distributed by: Novartis Pharmaceuticals Corporation East Hanover, NJ 07936 Product of Ireland, NDC 0078-0972-61.

Recalling firm
Novartis Pharmaceuticals Corp.
NDC code
0078-0972-61
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1309-2019

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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