Marketed Without An Approved NDA/ANDA: Parenteral product is labeled for use as an antidote.
Marketed Without An Approved NDA/ANDA: Parenteral product is labeled for use as an antidote.
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 Flawless Beauty LLC to request your refund or repair — edit it as you like.
Subject: Recall D-1318-2014 — Flawless Beauty LLC Flawless Beauty LLC recalls Saluta (reduced glutathione) Powder for Injection, Hello, I own a Flawless Beauty LLC recalls Saluta (reduced glutathione) Powder for Injection, 600 mg/vial, packaged in 10 vials per box, Exclusively Distributed that is covered by recall D-1318-2014 from Flawless Beauty LLC. 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.
