Reported Jan 22, 2014 · Terminated

GLUCOSAMINE/CHONDROITIN DS, Capsule, 500 mg/400 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC…

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?

  • GLUCOSAMINE/CHONDROITIN DS, Capsule, 500 mg/400 mg, Over The Counter
  • Distributed byAidaPak Service, LLC, NDC 00904548152
Lot codes and dates
  • GLUCOSAMINE/CHONDROITIN DS, Capsule, 500 mg/400
  • mg has the following codes PedigreeAD21846_14
  • EXP5/1/2014
  • PedigreeW003316
  • EXP6/18/2014
  • PedigreeAD73521_16
  • EXP5/30/2014
Amount recalled
180 Capsules

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; GLUCOSAMINE/CHONDROITIN DS, Capsule, 500 mg/400 mg may be potentially mislabeled as GLYCOPYRROLATE, Tablet, 2 mg, NDC 00603318121, Pedigree: AD22865_4, EXP: 5/2/2014; PREGABALIN, Capsule, 25 mg, NDC 00071101268, Pedigree: W003121, EXP: 6/13/2014; MULTIVITAMIN/MULTIMINERAL, Chew Tablet, NDC 00536344308, Pedigree: AD73521_10, EXP: 5/30/2014.

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

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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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, 7:45 PM UTC

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