Aidapak Recalls Hydrochlorothiazide Tablets Due to Potential Label Mixup
Aidapak Services, LLC is recalling Hydrochlorothiazide 12.5 mg tablets because they may have been mislabeled as other prescription drugs.
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 minor labeling errors or low-risk contamination where the probability of serious adverse health consequences is remote. No illnesses or injuries are reported in the source text.
Plain-English summary
Aidapak Services, LLC is recalling Hydrochlorothiazide, Tablet, 12.5 mg, NDC 00228282011. The recall was initiated because the medication may have been mislabeled as either hydrALAZINE HCl, Tablet, 100 mg, or CLINDAMYCIN HCL, Capsule, 300 mg.
The affected Hydrochlorothiazide tablets were repacked and distributed in Arizona, California, Oregon, and Washington. The specific lots involved include pedigree AD73652_7 with an expiration date of 5/29/2014, and pedigree AD67989_13 with an expiration date of 5/28/2014.
Consumers and healthcare providers should check their inventory for these specific lot numbers and expiration dates. If the medication is found, it should be returned to the pharmacy or distributor for replacement or refund. Patients should consult their healthcare provider if they have questions regarding their medication.
The recalled product
- Product
- HYDROCHLOROTHIAZIDE, Tablet, 12.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00228282011.
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Prescription Medication
- Hazard
- Affected units
- 300
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 (5)
- HYDROCHLOROTHIAZIDE
- Tablet
- 12.5 mg has the following codes: Pedigree: AD73652_7
- EXP: 5/29/2014 Pedigree: AD67989_13
- EXP: 5/28/2014
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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