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Use caution Drug recall · FDA · Published August 30, 2016

Actavis Ramipril Recall: Incorrect Expiration Date on Bottles

Actavis recalls 15,984 bottles of Ramipril 1.25 mg capsules due to incorrect expiration dates. Check your lot number and expiry date immediately.

🇺🇸 FDA recall #D-0118-2017DrugActavis ›
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Recalling firmActavis Laboratories, FL, Inc.4955 Orange Dr · Davie, FL 33314-3902
✎ GovInfoNow plain-language explainer

What happened, in plain English

Actavis Laboratories is recalling 15,984 bottles of Ramipril Capsules, USP, 1.25 mg because the labeling shows an incorrect expiration date. The affected bottles are labeled with an expiration date of 03/18 instead of the correct date of 09/17. This error means consumers cannot accurately determine if the medication is still within its approved shelf life. Read more at govinfonow.com/recall/42463-actavis-ramipril-recall-incorrect-expiration-date-on-bottles.

Source Summary by GovInfoNow · govinfonow.com/recall/42463-actavis-ramipril-recall-incorrect-expiration-date-on-bottles · Updated October 11, 2026 · FDA enforcement record: FDA #D-0118-2017

Cite this page

“Actavis Ramipril Recall: Incorrect Expiration Date on Bottles.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/42463-actavis-ramipril-recall-incorrect-expiration-date-on-bottles. Based on FDA recall #D-0118-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0118-2017%22&limit=1).

Why it’s dangerous

The primary hazard is the discrepancy between the printed expiration date (03/18) and the actual expiration date (09/17). While the record does not state the medication is unsafe, an incorrect date prevents users from knowing when the drug actually expires. Using medication past its true expiration date can reduce its effectiveness or alter its chemical stability.

Who’s affected

Consumers who purchased Ramipril Capsules, USP, 1.25 mg in 30-count bottles distributed nationwide and in Puerto Rico before August 30, 2016. Patients relying on this specific lot may be at risk of using medication past its verified expiration.

How to tell if you have this one

Check your bottle for the following details: Product name Ramipril Capsules, USP, 1.25 mg; 30-count bottle; NDC 16252-570-30; Lot # 1136091A; and an incorrect expiration date of 03/18 printed on the label.

  • Brand
    Actavis
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Your Bottle

    Verify if your bottle matches Lot # 1136091A and has an expiration date of 03/18.

  2. Contact Pharmacy or Manufacturer

    If you have the recalled lot, contact your pharmacy or Actavis for instructions on returning or disposing of the product.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFLPuerto Rico: yesPR

FDA distribution: “Nationwide and Puerto Rico” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 2 months after the firm started it.

1. Firm started the recall: Aug 30, 201612. FDA classified it Class III: Nov 1, 201623. Published in FDA’s Enforcement Report: Nov 9, 201632016
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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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-0118-2017 (August 30, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0118-2017 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA