Failed Impurities/Degradation Specifications: Product recalled due to elevated impurity result detected during routine stability testing.
Failed Impurities/Degradation Specifications: Product recalled due to elevated impurity result detected during routine stability testing.
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 Bio-pharm, Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-0809-2016 — Bio-pharm, Inc. Bio-pharm, Inc. recalls Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL Hello, I own a Bio-pharm, Inc. recalls Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL (75 mg/5 mL), 16 fl oz Bottle, Rx only, Mfd For: Heritage that is covered by recall D-0809-2016 from Bio-pharm, 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.
