Lack of Assurance of Sterility: all sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility assurance and concerns associated with the quality control processes.
Lack of Assurance of Sterility: all sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility assurance and concerns associated with the quality control processes.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send FVS Holdings, Inc. dba. Green Valley Drugs to request your refund or repair — edit it as you like.
Subject: Recall D-350-2013 — FVS Holdings, Inc. dba. Green Valley Drugs FVS Holdings, Inc. dba. Green Valley Drugs recalls Biotin Hello, I own a FVS Holdings, Inc. dba. Green Valley Drugs recalls Biotin Injection, all strengths and all presentations including Biotin-15-30 mL, Rx only, Green Valley Drugs, 1850 that is covered by recall D-350-2013 from FVS Holdings, Inc. dba. Green Valley Drugs. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
