Venlafaxine HCL Tablets Recalled for Potential Labeling Errors
Aidapak Services, LLC is recalling Venlafaxine HCL 25 mg tablets because they may have been mislabeled as other prescription drugs.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a prescription drug labeling error where the medication could be mistaken for other drugs with different dosages and therapeutic profiles, posing a risk of harm if the wrong medication is administered, which aligns with the 'High' severity criteria for risk-of-harm products.
Plain-English summary
Aidapak Services, LLC is recalling Venlafaxine HCL, Tablet, 25 mg (NDC 00093019901) due to a labeling error. The recalled tablets may have been mislabeled as sitagliptin phosphate 50 mg, levothyroxine sodium 112 mcg, or lithium carbonate ER 450 mg.
The repacked drugs were distributed in Arizona, California, Oregon, and Washington. The specific pedigree codes and expiration dates for the affected Venlafaxine HCL tablets are W002825 (EXP: 12/31/2013), W003860 (EXP: 6/27/2014), and AD62796_4 (EXP: 5/22/2014).
Patients and healthcare providers should check their medication labels and contact their pharmacist or physician if they have received Venlafaxine HCL 25 mg tablets that may be mislabeled as one of the other listed drugs.
The recalled product
- Product
- VENLAFAXINE HCL, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093019901.
- 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)
- VENLAFAXINE HCL
- Tablet
- 25 mg has the following codes: Pedigree: W002825
- EXP: 12/31/2013
- Pedigree: W003860
- EXP: 6/27/2014
- Pedigree: AD62796_4
- EXP: 5/22/2014.
Distribution
Part of a larger recall action
This product is one of 265 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 265 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