Aidapak Recalls Multivitamin Tablets Due to Potential Labeling Errors
Aidapak Services is recalling specific lots of multivitamin tablets because they may be mislabeled as other prescription medications.
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 temporary or medically reversible adverse health consequence. The hazard is a labeling mixup, which fits the criteria for moderate severity involving labeling errors.
Plain-English summary
Aidapak Services, LLC is recalling specific lots of MULTIVITAMIN/MULTIMINERAL LOW IRON Tablets (NDC 64376081601). The recall is due to a labeling mixup where these over-the-counter tablets may be potentially mislabeled as other prescription drugs, including Levothyroxine Sodium, Atorvastatin Calcium, or a different Multivitamin/Multimineral product.
The affected repacked drugs were distributed in Arizona, California, Oregon, and Washington. The specific lots involved have pedigree codes AD60272_31, AD73627_8, and W002507, with expiration dates of May 22, 2014, May 30, 2014, and June 3, 2014, respectively.
Consumers should check their medication bottles for these specific NDC numbers and pedigree codes. If the product matches the recalled description, they should stop using it and contact their pharmacist or the recalling firm for instructions on disposal or replacement.
The recalled product
- Product
- MULTIVITAMIN/MULTIMINERAL LOW IRON Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 64376081601
- Manufacturer
- Aidapak Services, LLC
- Hazard
- Affected units
- 400
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 (5)
- EXP: 5/22/2014
- Pedigree: AD73627_8
- EXP: 5/30/2014
- Pedigree: W002507
- EXP: 6/3/2014.
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.
See all 273 products in this recall →Related recalls
Same manufacturer · Aidapak Services, LLC
See all →- ModerateAidapak Recalls Sennosides Tablets Due to Potential Labeling Errors
FDA (Drugs) · 2014-01-29
- ModerateLevothyroxine Sodium Tablets Recalled for Potential Labeling Mixup
FDA (Drugs) · 2014-01-29
- ModerateAidapak Recalls Mislabeled Pantoprazole Sodium DR Tablets
FDA (Drugs) · 2014-01-29
- ModerateAidapak Recalls Nifedipine ER Tablets Due to Potential Label Mixup
FDA (Drugs) · 2014-01-29
- ModerateSimvastatin Tablets Recalled for Potential Labeling Error
FDA (Drugs) · 2014-01-29
Same hazard · mis labeling
See all →- ModerateMedline Trach Tube Kit Recalled for Component Labeling Discrepancy
FDA (Devices) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- ModerateOlympus Recalls PowerSeal Sealer Due to Incorrect Outer Box Labeling
FDA (Devices) · 2026-09-02
- HighSura Tanmen Ramen Noodles Recalled for Undeclared Fish Allergens
FDA (Food) · 2026-09-02
- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-09-02