Aidapak Recalls Multivitamin Capsules Due to Potential Label Mixup
Aidapak Services, LLC is recalling specific lots of multivitamin capsules that may be mislabeled as caffeine or melatonin 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 (label mixup) without reported injuries or illnesses, fitting the criteria for moderate severity.
Plain-English summary
Aidapak Services, LLC is recalling specific lots of MULTIVITAMIN/ MULTIMINERAL/ LUTEIN Capsules, 204-count bottles, due to a potential label mixup. The recalled product is an over-the-counter supplement distributed in Arizona, California, Oregon, and Washington.
The recall was initiated because the multivitamin capsules may be mislabeled as CAFFEINE, Tablet, 200 mg, or MELATONIN, Tablet, 3 mg. The source text identifies specific pedigree codes and expiration dates for the affected multivitamin lots, as well as the pedigree codes for the potentially mislabeled caffeine and melatonin products.
Consumers should check their medication cabinets for the specific pedigree codes and expiration dates listed in the official recall notice. If the product matches the recalled description, consumers should stop using it and contact the recalling firm for instructions on return or disposal.
The recalled product
- Product
- MULTIVITAMIN/ MULTIMINERAL/ LUTEIN Capsule, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 24208063210
- Manufacturer
- Aidapak Services, LLC
- Hazard
- Affected units
- 204
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 (7)
- EXP: 5/2/2014
- Pedigree: AD60240_45
- EXP: 5/22/2014
- Pedigree: W003025
- EXP: 6/12/2014
- Pedigree: AD73521_37
- EXP: 5/30/2014.
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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