Aidapak Recalls Levothyroxine Sodium Tablets Due to Labeling Errors
Aidapak Services is recalling Levothyroxine Sodium tablets because they may have been mislabeled as other prescription drugs.
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, which typically involves a labeling error that could result in temporary or medically reversible health consequences. No injuries or illnesses are reported in the source text.
Plain-English summary
Aidapak Services, LLC is recalling Levothyroxine Sodium tablets, 88 mcg, NDC 00781518392. The recall is due to a labeling error where the product may have been mislabeled as other prescription medications, including clomipramine HCl, hydroxychloroquine sulfate, or hyoscyamine sulfate.
The affected repacked drugs were distributed in Arizona, California, Oregon, and Washington. Specific pedigree codes and expiration dates are listed in the recall notice for identification.
Consumers should check their medication labels and contact their healthcare provider or pharmacist if they have questions about the product. Do not take the medication if the label does not match the prescription.
The recalled product
- Product
- LEVOTHYROXINE SODIUM, Tablet, 88 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00781518392.
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Prescription Medication
- Hazard
- Affected units
- 360
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 (10)
- LEVOTHYROXINE SODIUM
- Tablet
- 88 mcg has the following codes: Pedigree: AD46265_34
- EXP: 5/15/2014
- Pedigree: AD70629_13
- EXP: 5/29/2014
- Pedigree: W003439
- EXP: 6/20/2014
- Pedigree: AD60272_73
- EXP: 5/22/2014.
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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