FDA recall record

Town and Country Compounding and Consultation Sermorelin/GHRP-6 Injection 6 mg-3 mg recall — FDA D-0228-2017

Non-Sterility; microbial contamination identified as Bacillus circulans

Class Iclassification
D-0228-2017official record ID
Dec 28, 2016report date

Recall record at a glance

Official recordD-0228-2017
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmTown and Country Compounding and Consultation Services
Report dateDec 28, 2016
Recall initiation dateAug 1, 2016
Quantity12 vials
LocationRidgewood, NJ, United States

Official product description

Sermorelin/GHRP-6 Injection 6 mg-3 mg Lyophylized I, 2 mL vial, Rx, Town and Country Compounding and Consultation Services, Ridgewood, NJ 074502

Why the product was recalled

Non-Sterility; microbial contamination identified as Bacillus circulans

Distribution information

MA, NY, NJ & FL; Canada

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement 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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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