Bromocriptine Mesylate Tablets Recalled for Potential Labeling Error
Aidapak Services is recalling Bromocriptine Mesylate 2.5 mg tablets because they may have been mislabeled as Cyanocobalamin 1000 mcg.
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 moderate severity.
Plain-English summary
Aidapak Services, LLC is recalling Bromocriptine Mesylate, Tablet, 2.5 mg (NDC 00781532531) due to a potential labeling error. The source text indicates that these tablets may have been mislabeled as CYANOCOBALAMIN, Tablet, 1000 mcg (NDC 00904421713).
The affected product is identified by the pedigree AD32579_7 and an expiration date of 5/9/2014. The repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Consumers should check their medication for the specific NDC and pedigree listed above. If the product matches the description, they should contact their pharmacist or healthcare provider for guidance on proper disposal or replacement.
The recalled product
- Product
- BROMOCRIPTINE MESYLATE, Tablet, 2.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00781532531.
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Prescription Medication
- Hazard
- Affected units
- 30
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)
- BROMOCRIPTINE MESYLATE
- Tablet
- 2.5 mg has the following codes: Pedigree: AD32579_7
- 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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