Zolpidem Tartrate Tablets Recalled for Potential Labeling Error
Aidapak Services is recalling Zolpidem Tartrate tablets that may be mislabeled as Temazepam capsules due to a label mixup.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a potential mislabeling of a prescription drug as a different medication, which poses a risk of harm if the wrong drug is administered, but no injuries or illnesses have been reported.
Plain-English summary
Aidapak Services, LLC is recalling Zolpidem Tartrate tablets, 2.5 mg, NDC 64679071401. The recall is due to a labeling error where the product may be mislabeled as Temazepam capsules, 7.5 mg, NDC 00378311001.
The affected product is identified by Pedigree AD28355_1 and an expiration date of 5/8/2014. The repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Consumers should check their medication for the specific NDC and pedigree codes listed above. If the product matches the description, they should contact their pharmacist or healthcare provider for guidance on disposal or replacement.
The recalled product
- Product
- ZOLPIDEM TARTRATE, Tablet, 2.5 mg (1/2 of 5 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 64679071401
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Prescription Medication
- Hazard
- Affected units
- 402
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 (3)
- ZOLPIDEM TARTRATE Tablet
- 2.5 mg (1/2 of 5 mg) has the following code Pedigree: AD28355_1
- EXP: 5/8/2014.
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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