Glycopyrrolate Tablets Recalled for Potential Labeling Error
Aidapak Services is recalling Glycopyrrolate 2 mg tablets because they may be mislabeled as Lactobacillus tablets.
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 and involves a labeling error (mislabeling) without reported injuries or illnesses, fitting the criteria for a moderate severity score.
Plain-English summary
Aidapak Services, LLC is recalling Glycopyrrolate Tablets, 2 mg, NDC 49884006601. The recall is due to a labeling error where the product may be mislabeled as Lactobacillus Tablets, NDC 64980012950.
The affected product is identified by Pedigree W003625 and an expiration date of 6/25/2014. The repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Consumers should check their medication for the specific NDC and pedigree number listed above. If the product matches the description, they should contact their healthcare provider or pharmacist for guidance on how to proceed.
The recalled product
- Product
- GLYCOPYRROLATE Tablet, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 49884006601
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Tablets
- 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)
- GLYCOPYRROLATE
- Tablet
- 2 mg has the following code Pedigree: W003625
- EXP: 6/25/2014.
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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