Enalapril Maleate, USP 5MG, 90-count bottle, RX only. Packaged By: Aidarex Pharmaceuticals. Mfg: ...

FDA Drug Recall #D-0991-2018 — Class III — June 27, 2018

Recall Summary

Recall Number D-0991-2018
Classification Class III — Low risk
Date Initiated June 27, 2018
Status Terminated
Voluntary Voluntary: Firm initiated

Recalling Firm

Firm Aidarex Pharmaceuticals LLC
Location Corona, CA
Product Type Drugs
Quantity 61, 90-count bottles

Product Description

Enalapril Maleate, USP 5MG, 90-count bottle, RX only. Packaged By: Aidarex Pharmaceuticals. Mfg: Wockhardt Ltd. India. NDC: 33261-0693-90

Reason for Recall

Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.

Distribution Pattern

Distributed Nationwide in the USA

Lot / Code Information

Lots: 51904-1, EXP: 01/31/2018; 51904-4, 52885-1, EXP: 03/31/2018; 52885-3, EXP: 04/30/2018; 52885-4,EXP: 05/28/2018; 53840-2,EXP: 5/28/2018; 53840-3, EXP:6/30/2018; 53840-4, EXP:8/31/2018; 56665-1, EXP: 01/31/2019; 58596-1, EXP: 05/28/2019.

Other Recalls from Aidarex Pharmaceuticals LLC

Recall # Classification Product Date
D-0992-2018 Class III Enalapril Maleate, USP 5MG, 30-count bottle, RX... Jun 27, 2018
D-0990-2018 Class III Enalapril Maleate, USP 2.5MG, 90-count bottle, ... Jun 27, 2018
D-0810-2018 Class III Ferrous Sulfate 325 MG tablet; NDC 33261-0715-00 Apr 10, 2018
D-1162-2017 Class III Phentermine, USP Capsules, 15 mg, 30 count bott... Sep 5, 2017
D-0053-2018 Class III ENALAPRIL MALEATE Tablets, USP, 5MG, 90-count b... Sep 5, 2017

Frequently Asked Questions

Stop taking the medication and contact your pharmacist or doctor immediately. For Class I recalls, this is urgent. For Class II or III recalls, consult your doctor before stopping — abruptly discontinuing certain medications (blood pressure drugs, antidepressants, diabetes medications) can be more harmful than continuing while arranging a replacement. Check whether the recall applies to your specific lot number and expiration date. Return the product to your pharmacy and report any adverse effects to FDA MedWatch at 1-800-FDA-1088.

Not necessarily. Many drug recalls are initiated because of quality system failures or test results that suggest a product might not meet specifications — even if no patients have reported harm. The FDA uses a precautionary approach: if there is reason to believe quality standards were not met, a recall is required regardless of whether adverse effects have been reported. Class I recalls typically involve a reasonable probability of harm; Class II recalls may cause temporary health issues; Class III recalls are for products unlikely to cause adverse health consequences but that still violate regulations.

Pharmacies typically receive recall notices directly from drug wholesalers and manufacturers within days of the recall being announced. Your pharmacist can look up whether any product in your prescription history matches a recalled lot number. For current recalls, the FDA publishes updates at FDA.gov/safety/recalls-market-withdrawals-safety-alerts and sends MedWatch email alerts for significant drug safety issues. You can sign up for MedWatch alerts at FDA.gov. Most major pharmacy chains also have their own recall notification systems that automatically alert pharmacists when a recalled product is in their inventory.

What Should You Do?

Stop using this medication if affected by this recall. Contact your pharmacist or prescribing doctor immediately for guidance. Do not flush medications — use a drug take-back program.