FDA recall record

Talon Compounding Pharmacy Sermorelin 6 mg and Sermorelin 6 mg/GHRP-2 Injection, 12 mg, 10 recall — FDA D-1463-2016

Lack of Assurance of Sterility

Class IIclassification
D-1463-2016official record ID
Aug 31, 2016report date

Recall record at a glance

Official recordD-1463-2016
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmTalon Compounding Pharmacy
Report dateAug 31, 2016
Recall initiation dateJul 19, 2016
Quantity500 vials
LocationSan Antonio, TX, United States

Official product description

Sermorelin 6 mg and Sermorelin 6 mg/GHRP-2 Injection, 12 mg, 10 ml depyrogenated vials, Rx Only, Compounded by Talon Compounding Pharmacy, San Antonio, TX 78247

Why the product was recalled

Lack of Assurance of Sterility

Distribution information

Nationwide

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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