Aidapak Recalls aMILoride Tablets Due to Potential Label Mixup
Aidapak Services, LLC is recalling aMILoride HCl 5 mg tablets because they may be mislabeled as Propranolol HCl 10 mg or Famotidine 20 mg.
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 lead to a temporary or medically reversible adverse health consequence. The rubric assigns a score of 2 to minor labeling errors and low-risk contamination.
Plain-English summary
Aidapak Services, LLC is recalling aMILoride HCl Tablet, 5 mg, Rx only, NDC 64980015101. The recall is due to a labeling error where the product may be mislabeled as PROPRANOLOL HCL, Tablet, 10 mg, NDC 23155011001, or FAMOTIDINE, Tablet, 20 mg, NDC 16714036104.
The affected aMILoride HCl tablets have the following pedigree and expiration codes: Pedigree AD60272_55, EXP 5/22/2014, and Pedigree W003686, EXP 6/26/2014. The repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Consumers and healthcare providers should check their inventory for these specific codes and stop using the product if it matches the description. They should contact their pharmacist or the recalling firm for instructions on returning the product.
The recalled product
- Product
- aMILoride HCl Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64980015101
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Prescription Medication
- Hazard
- Affected units
- 200
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 (6)
- aMILoride HC
- Tablet
- 5 mg has the following codes Pedigree: AD60272_55
- EXP: 5/22/2014
- Pedigree: W003686
- 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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