US Drug Recall Register
Class II · Moderate risk Terminated Initiated Sep 10, 2018 (8 years ago)

HCG 6000 unit/0.3 gm Mannitol Lyopholized 6000 IU/vial injectable, Pharm D Solutions…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of Assurance of Sterility

What was recalled

HCG 6000 unit/0.3 gm Mannitol Lyopholized 6000 IU/vial injectable, Pharm D Solutions, Houston, Texas --- NDC 69699-1739-06

Recalling firm
Pharm D Solutions, LLC
NDC code
69699-1739-06
Origin
TX, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0164-2019

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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