Aidapak Recalls Pyridoxine HCL Tablets Due to Potential Label Mixup
Aidapak Services, LLC is recalling Pyridoxine HCL 25 mg tablets because they may have been mislabeled as Torsemide 10 mg.
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, which corresponds to a Severe severity score under the rubric, particularly given the risk of administering the wrong medication.
Plain-English summary
Aidapak Services, LLC is recalling Pyridoxine HCL, Tablet, 25 mg, Over The Counter, NDC 00536440601. The recall is due to a labeling error where the product may have been mislabeled as Torsemide, Tablet, 10 mg, NDC 50111091601.
The affected product is identified by the pedigree AD30197_28 and an expiration date of 5/9/2014. The repacked drugs were distributed in Arizona, California, Oregon, and Washington. The recall is classified as FDA Class II.
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 guidance.
The recalled product
- Product
- PYRIDOXINE HCL, Tablet, 25 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536440601.
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Tablets
- Hazard
- Affected units
- 102
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)
- PYRIDOXINE HCL
- Tablet
- 25 mg has the following codes: Pedigree: AD30197_28
- EXP: 5/9/2014.
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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