Wockhardt Limited recalls Enalapril Maleate Tablets USP; 5 mg NDC code 64679-924-03. 1000 Tablets HDPE container pack with Non CRC cap and 2
Wockhardt recalls 5mg enalapril tablets with failed impurities/degradation specs. Batch numbers listed; affected units may cause health risks. Contact for remedy.
Lower-risk recall
Failed Impurities/Degradation Specifications
Contact the company & request your remedy
What happened, in plain English
Wockhardt is recalling 5mg enalapril maleate tablets due to failed impurities or degradation specifications. This could pose health risks to users, so affected individuals should stop using the product. Read more at govinfonow.com/recall/40434-wockhardt-enalapril-5mg-tablets-recall-failed-impurities-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/40434-wockhardt-enalapril-5mg-tablets-recall-failed-impurities-risk · Updated October 6, 2026 · FDA enforcement record: FDA #D-0912-2018
Cite this page
“Wockhardt Enalapril 5mg Tablets Recall: Failed Impurities Risk.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/40434-wockhardt-enalapril-5mg-tablets-recall-failed-impurities-risk. Based on FDA recall #D-0912-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0912-2018%22&limit=1).
Why it’s dangerous
The tablets may contain impurities or degrade over time, potentially causing health issues. This is a quality control failure in the manufacturing process.
Who’s affected
People who purchased the recalled enalapril tablets from pharmacies or online retailers. Those with high blood pressure or on related medication are most at risk.
How to tell if you have this one
Check for the NDC code 64679-924-03 on the packaging. The product includes 1000 tablets in an HDPE container with a non-CRC cap and desiccants. Batch numbers listed in the recall include DR10445 through DS10048 with expiration dates up to December 2019.
- Brand
Wockhardt- Category
Drug
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class III- Status
Terminated- Distribution
Nationwide.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0912-2018 | Enalapril Maleate Tablets USP; 5 mg NDC code 64679-924-03. 1000 Tablets HDPE container pack with Non CRC cap and 2 desiccants further packed in E-flute cartons.; Batch# DR10445 (Exp: 4/19); Batch# DR10637 (Exp: 5/19); Batch# DR10646 (Exp: 5/19); Batch# DR10647 (Exp: 5/19); Batch# DR10725 (Exp: 7/19); Batch# DR10755 (Exp: 7/19); Batch# DR10811 (Exp: 9/19); Batch# DS10040 (Exp: 12/19); Batch# DS10041 (Exp: 12/19); Batch# DS10024 (Exp: 12/19); and Batch# DS10048 (Exp: 12/19). | 31,710 tablets |
| D-0913-2018 | Enalapril Maleate Tablets USP; 2.5 mg NDC code 64679-923-03. 1000 Tablets HDPE container pack with Non CRC cap and 2 desiccants further packed in E-flute cartons.; Batch# DR10447 (Exp: 4/19); Batch# DR10996 (Exp: 10/19); Batch# DS10201 (Exp: 2/20); and Batch# DR10319 (Exp: 3/20). | 17,628 tablets |
What to do — step by step
Check Product Details
Look for the NDC code 64679-924-03 and batch numbers listed in the recall (DR10445 to DS10048) on the packaging.
Questions people ask
Why is this product being recalled?
The tablets failed impurities or degradation specifications, which could pose health risks.
How do I know if I have the recalled product?
Check for the NDC code 64679-924-03 and batch numbers DR10445 through DS10048 on the packaging.
What should I do if I have the recalled product?
The recall record does not specify a remedy, so contact Wockhardt Limited for further instructions.
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-0912-2018 — Wockhardt Wockhardt Hello, I own a Wockhardt that is covered by recall D-0912-2018 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-0912-2018 (June 19, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0912-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 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.