FDAClass IDecember 28, 2016

Sermorelin/GHRP-6 Injection 6 mg-3 mg Lyophylized I recall: Sterility Concern

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 was Sermorelin/GHRP-6 Injection 6 mg-3 mg Lyophylized I recalled?

Non-Sterility; microbial contamination identified as Bacillus circulans

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 #07172016@1, exp 1/13/2017

Product
Sermorelin/GHRP-6 Injection 6 mg-3 mg Lyophylized I, 2 mL vial, Rx, Town and Country Compounding and Consultation Services, Ridgewood, NJ 074502
Recalling firm
Town and Country Compounding and Consultation Services
Quantity
12 vials
Distribution
MA, NY, NJ & FL; Canada
Recall date
December 28, 2016
Classification
Class I
Status
Terminated
Agency
FDA (drug)
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