Class II · Moderate risk Terminated
Artridon Glucosamine
Reason CGMP Deviations
GLUCOSAMINE/CHONDROITIN Capsule
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Labeling:Label Mixup; GLUCOSAMINE/CHONDROITIN Capsule, 500 mg/400 mg may be potentially mislabeled as FEXOFENADINE HCL, Tablet, 60 mg, NDC 45802042578, Pedigree: AD60240_30, EXP: 5/22/2014.
What was recalled
GLUCOSAMINE/CHONDROITIN Capsule, 500 mg/400 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 54458010022
- Recalling firm
- Aidapak Services, LLC
- Origin
- WA, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-616-2014
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Glucosamine recalls
See all
Class II · Moderate risk Ongoing
NaturesPlus Advanced Therapeutics Glucosamine Chondroitin MSM…
Reason MICROBIAL CONTAMINATION OF NON-STERILE PRODUCT: microbial contaminant identified as Pluralibacter gergoviae.
Class II · Moderate risk Ongoing
Glucosamine 200 mg/mL
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated
Glucosamine HCL Injectable
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated
Glucosamine/Chondroitin Ds
Reason Labeling: Label Mixup; GLUCOSAMINE/CHONDROITIN DS, Tablet, 500 mg/400 mg may be potentially mislabeled as DOCUSATE SODIUM, Capsule, 250 mg, NDC 00536375701, Pedigree: AD60211_11, EXP: 5/22/2014.
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