Aidapak Recalls Propranolol HCL ER Capsules Due to Labeling Error
Aidapak Services, LLC is recalling Propranolol HCL ER capsules because they may have been mislabeled as Cinacalcet HCL 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 due to a labeling error (label mixup) which is a minor labeling error that may cause temporary or medically reversible adverse health consequences, fitting the Moderate severity criteria.
Plain-English summary
Aidapak Services, LLC is recalling Propranolol HCL ER, Capsule, 60 mg, NDC 00228277811. The recall was initiated because the medication may have been mislabeled as Cinacalcet HCL, Tablet, 30 mg, NDC 55513007330. The affected product has the pedigree AD54605_4 and an expiration date of 5/20/2014.
The repacked drugs were distributed in Arizona, California, Oregon, and Washington. This is a Class II recall, indicating that use of, or exposure to, the violative product may cause temporary or medically reversible adverse health consequences.
Consumers should check their medication for the specific NDC and pedigree listed above. If the product matches the description, they should stop using it and contact their pharmacist or healthcare provider for instructions on how to return the medication.
The recalled product
- Product
- PROPRANOLOL HCL ER, Capsule, 60 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00228277811.
- 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)
- PROPRANOLOL HCL ER
- Capsule
- 60 mg has the following codes: Pedigree: AD54605_4
- EXP: 5/20/2014.
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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