Etodolac Tablets Recalled for Potential Labeling Error
Aidapak Services is recalling Etodolac 400 mg tablets due to a potential label mixup with Pancrelipase DR capsules.
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, fitting the criteria for moderate severity.
Plain-English summary
Aidapak Services, LLC is recalling Etodolac 400 mg tablets (NDC 51672401801) because they may be potentially mislabeled as Pancrelipase DR capsules (NDC 00032121201). The affected product is identified by Pedigree W003734 and an expiration date of 6/26/2014.
The recall was initiated due to a labeling error, specifically a label mixup. The repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Consumers and healthcare providers should check their inventory for Etodolac 400 mg tablets with the specified pedigree and expiration date. If found, these products should be returned to the pharmacy or distributor for replacement or refund.
The recalled product
- Product
- ETODOLAC Tablet, 400 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 51672401801
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Prescription Medication
- Hazard
- Affected units
- 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 (4)
- ETODOLAC
- Tablet
- 400 mg has the following code Pedigree: W003734
- EXP: 6/26/2014.
Distribution
Part of a larger recall action
This product is one of 273 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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