Reported Jan 22, 2014 · Terminated

PRAMIPEXOLE DI-HCL Tablet, 1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16714058701

Aidapak Services, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Aidapak Services, LLC · 14301 Se 1st St · Vancouver, WA · 98684-3501

Is this the product you have?

  • PRAMIPEXOLE DI-HCL Tablet, 1 mg, Rx only
  • Distributed byAidaPak Service, LLC, NDC 16714058701
Lot codes and dates
  • PRAMIPEXOLE DI-HCL Tablet, 1
  • mg has the following code PedigreeW003150
  • EXP6/13/2014
Amount recalled
90 Tablets

This recall covers 273 products

The agency filed one notice per product. You are reading one of them; the other 272 are below.

260 more are in the archive.

Where it was sold

Why it was recalled

Labeling: Label Mixup; PRAMIPEXOLE DI-HCL, Tablet, 1 mg may be potentially mislabel as MISOPROSTOL, Tablet, 200 mcg, NDC 59762500801, Pedigree: W003117, EXP: 6/13/2014.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Feb 7, 2014 · Data as of Sep 19, 4:57 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.