CGMP deviations; repackaged product was recalled by the manufacturer because it was manufactured under the same conditions as products found to be sub-potent.
CGMP deviations; repackaged product was recalled by the manufacturer because it was manufactured under the same conditions as products found to be sub-potent.
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 PD-Rx Pharmaceuticals, Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-0005-2021 — PD-Rx Pharmaceuticals, Inc. PD-Rx Pharmaceuticals, Inc. recalls Nature-Throid 1 GR (65 mg), Each Ta Hello, I own a PD-Rx Pharmaceuticals, Inc. recalls Nature-Throid 1 GR (65 mg), Each Tablet Contains: Thyroid USP 1 GR (65 mg), Liothyronine (T3) 9 mcg, Levothyroxine (T4) that is covered by recall D-0005-2021 from PD-Rx Pharmaceuticals, 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.
