Aidapak Recalls Propranolol HCL Tablets Due to Potential Label Mixup
Aidapak Services, LLC is recalling Propranolol HCL 10 mg tablets that may be mislabeled as Pioglitazone HCL 15 mg. The repacked drugs were distributed in four western states.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II. Per the rubric, FDA Class II recalls are assigned a severity score of 4 (Severe), as they may cause temporary or medically reversible adverse health consequences.
Plain-English summary
Aidapak Services, LLC is recalling Propranolol HCL, Tablet, 10 mg (NDC 16714002104) due to a labeling error. The recall involves 100-tablet packages that may be potentially mislabeled as Pioglitazone HCL, Tablet, 15 mg (NDC 00093204856). The affected products have the pedigree code AD52778_73 and an expiration date of 5/21/2014.
The repacked drugs were distributed in Arizona, California, Oregon, and Washington. This recall is classified as FDA Class II, indicating a situation that might cause temporary or medically reversible adverse health consequences.
Consumers and healthcare providers should check their inventory for Propranolol HCL 10 mg tablets with the specified pedigree and expiration date. If found, these products should be returned to the distributor or disposed of according to local regulations. Patients should consult their healthcare provider if they have questions regarding their medication.
The recalled product
- Product
- PROPRANOLOL HCL, Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16714002104
- 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
- Tablet
- 10 mg has the following code Pedigree: AD52778_73
- EXP: 5/21/2014.
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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