FDAClass IIDecember 26, 2018

Human Chorionic Gonadotropin 3000 IU recall: Sterility Concern

Human Chorionic Gonadotropin 3000 IU, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054 1-844-263-6843 --- NDC: 69699-1738-10

Why was Human Chorionic Gonadotropin 3000 IU recalled?

Lack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intended to be sterile.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot: 10292018:21 Exp. 3/31/2019

Product
Human Chorionic Gonadotropin 3000 IU, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054 1-844-263-6843 --- NDC: 69699-1738-10
Recalling firm
Pharm D Solutions, LLC
Quantity
85 vials
Distribution
WA
Recall date
December 26, 2018
Classification
Class II
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls