Reported Jan 29, 2014 · Terminated

HYOSCYAMINE SULFATE SL, Tablet, 0.125 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00574025001.

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?

  • HYOSCYAMINE SULFATE SL, Tablet, 0.125 mg, Rx only
  • Distributed byAidaPak Service, LLC, NDC 00574025001
Lot codes and dates

7 of 7 products

Products covered by this recall
#Product as published
1Pedigree: AD21790_19, EXP: 5/1/2014
2Pedigree: AD46265_7, EXP: 5/15/2014
3Pedigree: W003679, EXP: 6/25/2014
4Pedigree: AD60272_16, EXP: 5/22/2014
5Pedigree: AD30140_10, EXP: 5/7/2014
6Pedigree: W003000, EXP: 6/11/2014
7Pedigree: W003326, EXP: 6/19/2014.
Amount recalled
909 Tablets

This recall covers 265 products

The agency filed one notice per product. You are reading one of them; the other 264 are below.

252 more are in the archive.

Where it was sold

Why it was recalled

Labeling: Label Mixup: HYOSCYAMINE SULFATE SL, Tablet, 0.125 mg may have potentially been mislabeled as one of the following drugs: guanFACINE HCl, Tablet, 2 mg, NDC 65162071310, Pedigree: AD21790_13, EXP: 5/1/2014; CYCLOBENZAPRINE HCL, Tablet, 5 mg, NDC 00591325601, Pedigree: AD46265_4, EXP: 5/15/2014; guanFACINE HCl, Tablet, 2 mg, NDC 65162071310, Pedigree: W003678, EXP: 6/25/2014; guanFACIN

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, 5:49 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.