Acyclovir Tablets Recalled Due to Potential Labeling Error
Aidapak Services, LLC is recalling Acyclovir 800 mg tablets that may have been mislabeled as Pantoprazole Sodium 20 mg.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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 (mislabeling) without reported injuries or illnesses, fitting the criteria for a moderate severity score.
Plain-English summary
Aidapak Services, LLC is recalling Acyclovir, Tablet, 800 mg, Rx only, NDC 00093894701. The recall is due to a labeling error where the product may have been mislabeled as Pantoprazole Sodium DR, Tablet, 20 mg, NDC 64679043304.
The affected product has the pedigree AD70629_1 and an expiration date of 5/29/2014. The repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Consumers and healthcare providers should check their inventory for Acyclovir 800 mg tablets with the specified pedigree and expiration date. If found, they should stop using the product and contact the recalling firm for instructions on return or disposal.
The recalled product
- Product
- ACYCLOVIR, Tablet, 800 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093894701.
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Prescription Medication
- Hazard
- Affected units
- 100
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)
- ACYCLOVIR
- Tablet
- 800 mg has the following codes: Pedigree: AD70629_1
- EXP: 5/29/2014.
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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