FDA Recalls Propranolol HCL Tablets Due to Potential Label Mixup
Aidapak Services, LLC is recalling Propranolol HCL 10 mg tablets because they may be mislabeled as Lactobacillus Acidophilus capsules.
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, which typically involves minor labeling errors or low-risk contamination where the probability of temporary or medically reversible health consequences is low.
Plain-English summary
The U.S. Food and Drug Administration (FDA) has issued a recall for Propranolol HCL Tablet, 10 mg, distributed by Aidapak Services, LLC. The recall is due to a labeling error where the tablets may be potentially mislabeled as Lactobacillus Acidophilus, Capsule.
The affected product is identified by NDC 23155011010, with pedigree AD65317_1 and an expiration date of 5/24/2014. The quantity involved is 1,999 tablets. The repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Consumers and healthcare providers should check their inventory for this specific product and stop using it if the label indicates Lactobacillus Acidophilus or if the NDC matches the recalled item. Patients should contact their healthcare provider for alternative treatment options if necessary.
The recalled product
- Product
- PROPRANOLOL HCL Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 23155011010
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Prescription Medication
- Hazard
- Affected units
- 1,999
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 (3)
- PROPRANOLOL HCL Tablet
- 10 mg has the following code Pedigree: AD65317_1
- EXP: 5/24/2014.
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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