Aidapak Recalls Lactase Enzyme Tablets Due to Potential Label Mixup
Aidapak Services, LLC is recalling Lactase Enzyme Tablets because they may be mislabeled as other medications. The recall covers 2,872 tablets 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 error (mislabeling) without reported illnesses or injuries, which aligns with the rubric for moderate severity involving minor labeling errors or low-risk contamination.
Plain-English summary
Aidapak Services, LLC is recalling 2,872 Lactase Enzyme Tablets, 3000 units, Over The Counter (NDC 24385014976). The recall is due to a labeling error where the tablets may be potentially mislabeled as other products, including Benzocaine/Menthol Lozenges, Acetaminophen/Aspirin/Caffeine Tablets, or Guaifenesin ER Tablets.
The affected repacked drugs were distributed in Arizona, California, Oregon, and Washington. The source text does not specify the exact number of affected units beyond the total quantity or report any illnesses or injuries associated with the mislabeling.
Consumers should check their medication labels for the specific NDC and pedigree codes listed in the recall notice. If the product matches the recalled description, consumers should stop using it and contact their pharmacist or the recalling firm for instructions on return or disposal.
The recalled product
- Product
- LACTASE ENZYME Tablet, 3000 units, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 24385014976
- Manufacturer
- Aidapak Services, LLC
- Hazard
- Affected units
- 2,872
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 (15)
- LACTASE ENZYME Tablet
- 3000 units has the following codes Pedigree: AD21846_31
- EXP: 5/1/2014
- Pedigree: W003721
- EXP: 6/26/2014
- Pedigree: AD30028_25
- EXP: 5/7/2014
- Pedigree: AD60240_36
- EXP: 5/22/2014
- Pedigree: W002700
- EXP: 6/5/2014
- Pedigree: AD46257_53
- EXP: 5/15/2014
- Pedigree: W003021
- EXP: 6/12/2014.
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