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Drug recall · FDA · Published October 13, 2015

Rx PAK recalls Donnatal (Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide) tablets, 100-count bottle, Rx

Labeling: Not elsewhere classified - Product label incorrectly lists Scopolamine Hydrocodone as an active ingredient on the side panel instead of Scopolamine Hydrobromide.

🇺🇸 FDA recall #D-0053-2016DrugRx PAK ›
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Recalling firmRx PAK4971 Southridge Blvd Ste 111-115, N/A · Memphis, TN 38141-8300
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
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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.

Source Page by GovInfoNow · govinfonow.com/recall/43578-rx-pak-recalls-donnatal-phenobarbital-hyoscyamine-sulfate-atropine-sulfate-scopolamine · Recall date October 13, 2015 · FDA enforcement record: FDA #D-0053-2016

Cite this page

“Rx PAK recalls Donnatal (Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide) tablets, 100-count bottle, Rx.” GovInfoNow, recall dated October 13, 2015. https://govinfonow.com/recall/43578-rx-pak-recalls-donnatal-phenobarbital-hyoscyamine-sulfate-atropine-sulfate-scopolamine. Based on FDA recall #D-0053-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0053-2016%22&limit=1).

How to tell if you have this one

  • Brand
    Rx PAK
  • Category
    Drug
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We’ve drafted a message you can send Rx PAK to request your refund or repair — edit it as you like.

Subject: Recall D-0053-2016 — Rx PAK Rx PAK recalls Donnatal (Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine H

Hello,

I own a Rx PAK recalls Donnatal (Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide) tablets, 100-count bottle, Rx that is covered by recall D-0053-2016 from Rx PAK.

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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Where this comes from

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.

  • Official source: FDA Recall #D-0053-2016 (October 13, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0053-2016 to see it in context.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA