Subpotent Drug: This lot is being recalled because of out-of-specification test results for Diphenhydramine citrate.
Subpotent Drug: This lot is being recalled because of out-of-specification test results for Diphenhydramine citrate.
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 Pfizer Us Pharmaceutical Group to request your refund or repair — edit it as you like.
Subject: Recall D-1166-2014 — Pfizer Us Pharmaceutical Group Pfizer Us Pharmaceutical Group recalls Advil PM Caplets, (Ibuprofen, Hello, I own a Pfizer Us Pharmaceutical Group recalls Advil PM Caplets, (Ibuprofen, 200 mg /Diphenhydramine citrate, 38 mg) 120 count bottle, OTC, Pfizer, Madison, NJ 07940 that is covered by recall D-1166-2014 from Pfizer Us Pharmaceutical Group. 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.
