FDAClass IIDecember 18, 2019

Glutamine/Arginine/Carnitine in all strengths recall

Glutamine/Arginine/Carnitine in all strengths, all doses and all packaging, AnazaoHealth Corporate 5710 Hoover Blvd Tampa, FL 33634.

Why was Glutamine/Arginine/Carnitine in all strengths recalled?

Lack of Processing Controls; Environmental sampling revealed 1 CFU (Colony Forming Unit) identified as Talaromyces rotundus, a fungi.

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?

All lots filled and dispensed 09/24-26/2019 remaining within expiry.

Product
Glutamine/Arginine/Carnitine in all strengths, all doses and all packaging, AnazaoHealth Corporate 5710 Hoover Blvd Tampa, FL 33634.
Recalling firm
Coast Quality Pharmacy, LLC dba Anazao Health
Quantity
17 vials
Distribution
Nationwide in the U.S.
Recall date
December 18, 2019
Classification
Class II
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls