Aidapak Recalls Chlordiazepoxide Capsules Due to Potential Labeling Errors
Aidapak Services is recalling 1,101 chlordiazepoxide capsules because they may have been mislabeled as other medications. The affected drugs were distributed in four western states.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II and involves a labeling error (label mixup) without reported injuries or illnesses, which aligns with the rubric for minor labeling errors or low-risk contamination.
Plain-English summary
Aidapak Services, LLC is recalling 1,101 capsules of chlordiazepoxide HCl, 25 mg, because the product may have been mislabeled as other drugs. The recall involves specific pedigree codes and expiration dates ranging from May 2014 to June 2014.
The potential mislabeling could result in the chlordiazepoxide capsules being identified as flecainide acetate tablets, calcium acetate capsules, or Lactobacillus GG capsules. This labeling error poses a risk of patients receiving the wrong medication.
The repacked drugs were distributed in Arizona, California, Oregon, and Washington. Patients and healthcare providers should check their inventory for the specific NDC and pedigree codes listed in the recall notice and discontinue use if the product matches the recalled items.
The recalled product
- Product
- chlordiazePOXIDE HCl, Capsule, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00555015902.
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Prescription Medication
- Hazard
- Affected units
- 1,101
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (7)
- chlordiazePOXIDE HCl
- Capsule
- 25 mg has the following codes: Pedigree: AD46333_4
- EXP: 5/16/2014
- Pedigree: AD49426_1
- Pedigree: W003194
- EXP: 6/13/2014.
Distribution
Part of a larger recall action
This product is one of 265 recalled by Aidapak Services, LLC under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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