Aidapak Recalls Mislabeled HydrALAZINE HCl Tablets
Aidapak Services, LLC is recalling hydrALAZINE HCl 50 mg tablets that may be mislabeled as CapsuleTOPRIL 12.5 mg tablets.
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 the source text describes a labeling mixup without reporting any specific injuries or illnesses, fitting the criteria for moderate severity.
Plain-English summary
Aidapak Services, LLC is recalling hydrALAZINE HCl Tablet, 50 mg, NDC 50111032801, due to a labeling error. The source text indicates that these tablets may be potentially mislabeled as CapsuleTOPRIL, Tablet, 12.5 mg, NDC 00143117101.
The affected product is identified by the pedigree AD52778_28 and an expiration date of 5/20/2014. The repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Consumers and healthcare providers should check their inventory for hydrALAZINE HCl 50 mg tablets with the specified pedigree and expiration date. If found, they should stop using the product and contact the recalling firm for instructions.
The recalled product
- Product
- hydrALAZINE HCl Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 50111032801
- 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)
- hydrALAZINE HCl
- Tablet
- 50 mg has the following code Pedigree: AD52778_28
- EXP: 5/20/2014.
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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