Failed Impurities/Degradation Specifications; high out of specification results obtained at the 9 month stability timepoint
Failed Impurities/Degradation Specifications; high out of specification results obtained at the 9 month stability timepoint
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 PAI Holdings, LLC. dba Pharmaceutical Associates Inc to request your refund or repair — edit it as you like.
Subject: Recall D-0015-2021 — PAI Holdings, LLC. dba Pharmaceutical Associates Inc PAI Holdings, LLC. dba Pharmaceutical Associat Hello, I own a PAI Holdings, LLC. dba Pharmaceutical Associates Inc recalls Citalopram Oral Solution, USP 20 mg/10 mL, 10 mL unit dose cups, Rx Only, Mfg for: Pharmaceutical Associates, Inc. that is covered by recall D-0015-2021 from PAI Holdings, LLC. dba Pharmaceutical Associates Inc. 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.
