Aidapak Recalls Trimethobenzamide Capsules Due to Potential Label Mixup
Aidapak Services is recalling Trimethobenzamide HCl capsules because they may be mislabeled as other medications. The affected 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, which typically involves a labeling error that could lead to a temporary or medically reversible health issue. The source does not report any illnesses or injuries, fitting the criteria for a moderate severity score.
Plain-English summary
Aidapak Services, LLC is recalling Trimethobenzamide HCl Capsules, 300 mg, NDC 53489037601. The recall is due to a labeling error where the product may be mislabeled as Gabapentin, Cholecalciferol, or Sodium Bicarbonate. The agency classifies this as a Class II recall.
The repacked drugs were distributed in Arizona, California, Oregon, and Washington. The source text identifies specific pedigree codes and expiration dates for the affected lots, including AD21858_10, AD70625_1, and W002976.
Consumers should check their medication labels for the specific NDC and pedigree codes listed in the recall notice. If the product matches the description, they should stop using it and contact their healthcare provider or pharmacist for guidance.
The recalled product
- Product
- TRIMETHOBENZAMIDE HCl Capsule, 300 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 53489037601
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Prescription Medication
- Hazard
- Affected units
- 300
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 (8)
- TRIMETHOBENZAMIDE HCl
- Capsule
- 300 mg has the following codes Pedigree: AD21858_10
- EXP: 5/1/2014
- Pedigree: AD70625_1
- EXP: 5/29/2014
- Pedigree: W002976
- EXP: 6/11/2014.
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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