Metoprolol Succinate ER Tablets Recalled for Potential Labeling Mixup
Aidapak Services, LLC is recalling Metoprolol Succinate ER 200 mg tablets due to a potential labeling mixup. The affected 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 and involves a labeling mixup. Per the rubric, minor labeling errors and voluntary precautionary recalls without reported injuries are typically rated as Moderate.
Plain-English summary
Aidapak Services, LLC is recalling Metoprolol Succinate ER Tablets, 200 mg, NDC 62037083301, due to a labeling mixup. The specific product involved is identified by pedigree AD73652_13 and an expiration date of 5/30/2014. The tablets are prescription-only and were repacked in quantities of 100 tablets.
The repacked drugs were distributed in Arizona, California, Oregon, and Washington. The recall is classified as Class II by the FDA, indicating a situation that might temporarily or reversibly affect health.
Consumers and healthcare providers should check their inventory for the specific pedigree and expiration date listed. If the product is found, it should be returned to the distributor or pharmacy for disposal or replacement. Patients should consult their healthcare provider if they have questions regarding their medication.
The recalled product
- Product
- METOPROLOL SUCCINATE ER Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 62037083301
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Cardiovascular
- 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 (2)
- METOPROLOL SUCCINATE ER Tablet
- 200 mg
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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