Wockhardt Usa Inc. recalls Enalapril Maleate tablets, USP, 5mg, 1000-count bottles, Rx only, Manufactured by: Wockhardt Limited H-14/2, M.I.D.C.
Wockhardt recalls 5mg enalapril tablets due to impurities. Affected products have specific NDC and lot numbers. Stop using if you have these items.
Recall notice
Failed Impurities/Degradation Specifications: 5mg strength being recalled for out of specification results for related compound.
Contact the company & request your remedy
What happened, in plain English
Wockhardt is recalling 5mg enalapril maleate tablets that may contain impurities. This could affect medication safety for people using these prescription drugs. Read more at govinfonow.com/recall/41332-wockhardt-enalapril-5mg-tablets-recall-impurities-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/41332-wockhardt-enalapril-5mg-tablets-recall-impurities-risk · Updated October 7, 2026 · FDA enforcement record: FDA #D-0051-2018
Cite this page
“Wockhardt Enalapril 5mg Tablets Recall: Impurities Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/41332-wockhardt-enalapril-5mg-tablets-recall-impurities-risk. Based on FDA recall #D-0051-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0051-2018%22&limit=1).
Why it’s dangerous
The tablets may have impurities that don't meet safety standards. This could lead to unsafe medication effects, though the exact risk isn't specified in the recall.
Who’s affected
People with a prescription for these enalapril tablets are affected. Those using the medication for blood pressure or heart conditions are most at risk.
How to tell if you have this one
Check for NDC 64679-924-03 or lot numbers DR10635/DR10636 with expiration dates of May 2019. These tablets are prescription-only and sold in 1000-count bottles.
- Brand
Wockhardt- Category
Drug
What to do — step by step
Check Product Details
Look for NDC 64679-924-03 or lot numbers DR10635/DR10636 with expiration dates of May 2019.
Questions people ask
Why is this product being recalled?
The tablets may contain impurities that don't meet safety standards, but the exact risk isn't specified in the recall.
Do I need to stop using these tablets?
The recall doesn't specify a stop-use instruction, so you should check the product details first.
What should I do if I have these tablets?
The recall doesn't provide specific action steps, so contact your doctor or pharmacist for advice.
Contact Wockhardt
We’ve drafted a message you can send Wockhardt to request your refund or repair — edit it as you like.
Subject: Recall D-0051-2018 — Wockhardt Wockhardt Hello, I own a Wockhardt that is covered by recall D-0051-2018 from Wockhardt. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0051-2018 (August 22, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0051-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.