Quinapril Tablets Recalled for Potential Mislabeling as Propranolol HCL
Aidapak Services, LLC is recalling Quinapril 40 mg tablets that may be mislabeled as Propranolol HCL 10 mg. The error involves a label mixup on repacked drugs.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II. Per the rubric, FDA Class II recalls are assigned a severity score of 4 (Severe), particularly given the risk of administering the wrong medication.
Plain-English summary
Aidapak Services, LLC is recalling Quinapril Tablet, 40 mg, NDC 31722-0270-90, due to a labeling error. The specific issue is a label mixup where Quinapril 40 mg tablets may be potentially mislabeled as Propranolol HCL, Tablet, 10 mg, NDC 16714-0021-04.
The affected product is identified by the pedigree AD52778_76 and an expiration date of 5/21/2014. The repacked drugs were distributed in Arizona, California, Oregon, and Washington. The recall is classified as Class II by the FDA.
Patients and healthcare providers should check their medication labels. If a patient has Quinapril 40 mg tablets with the pedigree AD52778_76 that are labeled as Propranolol HCL 10 mg, they should stop using the medication and contact their healthcare provider or pharmacist for guidance.
The recalled product
- Product
- QUINAPRIL Tablet, 40 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 31722027090
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Prescription Medication
- Hazard
- Affected units
- 90
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 (3)
- QUINAPRIL Tablet
- 40 mg has the following code Pedigree: AD52778_76
- EXP: 5/21/2014.
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 →- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-10-14
- SevereBetter Bakehouse Recalls Donutful Chocolate Dipped Vanilla Cake Donuts for Undeclared Milk
FDA (Food) · 2026-10-14
- HighFreshPoint Recalls Cranberry Chicken Salad Wedges for Undeclared Egg Allergen
FDA (Food) · 2026-10-14
- HighJ K Patisserie & Bakery LLC Recalls Croissants for Undeclared Egg
FDA (Food) · 2026-10-14
- LowMindray ePM Series Patient Monitor Manuals Recalled for Alarm Clarification
FDA (Devices) · 2026-10-14
Similar recalls
- SevereFDA Recalls Propranolol HCL Tablets Due to Potential Label Mixup
FDA (Drugs) · 2014-01-29
- SevereFDA Recalls Mislabeled Quinidine Sulfate Tablets Distributed by Aidapak
FDA (Drugs) · 2014-01-29
- ModerateAidapak Recalls Propranolol HCL ER Capsules Due to Labeling Error
FDA (Drugs) · 2014-01-29
- ModerateFDA Recalls Propafenone HCL Tablets Due to Potential Labeling Mixup
FDA (Drugs) · 2014-01-29
- ModerateAidapak Recalls Pyridoxine HCL Tablets Due to Potential Label Mixup
FDA (Drugs) · 2014-01-29
- ModerateAidapak Recalls Chlorthalidone Tablets Due to Potential Label Mixup
FDA (Drugs) · 2014-01-29