Potassium Acid Phosphate Tablets Recalled for Potential Label Mixup
Aidapak Services, LLC is recalling Potassium Acid Phosphate tablets due to a potential label mixup with prednisone. The repacked drugs were distributed in four western states.
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 situation that might cause temporary or medically reversible adverse health consequences. The hazard is a labeling error (label mixup) rather than a contamination or structural defect, and no injuries or illnesses are reported in the source text.
Plain-English summary
Aidapak Services, LLC is recalling Potassium Acid Phosphate, Tablet, 500 mg, NDC 00486111101, due to a potential label mixup. The source text indicates that the tablets may have been mislabeled as predniSONE, Tablet, 20 mg, NDC 00591544301.
The recalled product is a prescription-only medication distributed in 100-tablet quantities. The specific pedigree code for the recalled Potassium Acid Phosphate is AD52778_34, with an expiration date of 5/20/2014. The potentially mislabeled prednisone product has pedigree code AD56879_5 and an expiration date of 5/21/2014.
The repacked drugs were distributed in Arizona, California, Oregon, and Washington. Consumers and healthcare providers should check their inventory for these specific NDC numbers and pedigree codes. If the product is found, it should be returned to the distributor or disposed of according to local regulations, as the label error could lead to the administration of the wrong medication.
The recalled product
- Product
- POTASSIUM ACID PHOSPHATE, Tablet, 500 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00486111101.
- 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)
- POTASSIUM ACID PHOSPHATE
- Tablet
- 500 mg has the following codes: Pedigree: AD52778_34
- 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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