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Class III: unlikely to cause harmOngoing

Ascend Laboratories Dabigatran etexilate Capsules Recall

Dabigatran etexilate Capsules, 150 mg, 20-count carton (2x10), Rx only, Manufactured by…

Ascend Laboratories, LLC · Bedminster, NJ

Risk level
Class III
Reported by FDA
Jul 29, 2026
Recall ID
D-0736-2026
Check your lot numberHow we source this data

Summary

Ascend Laboratories recalled Dabigatran etexilate Capsules starting Jun 30, 2026. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-0736-2026 on Jul 29, 2026. Reason: Failed Impurities/Degradation Specifications: OOS result was observed during the related substance test analysis with respect to Impurity II, Impurity III and Total impurity testing for 12 Month Long-Term Stability. Status: Ongoing.

Why it was recalled

Failed Impurities/Degradation Specifications: OOS result was observed during the related substance test analysis with respect to Impurity II, Impurity III and Total impurity testing for 12 Month Long-Term Stability.

Product description

Dabigatran etexilate Capsules, 150 mg, 20-count carton (2x10), Rx only, Manufactured by: Alkem Laboratories, Mumbai, INDIA, Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268, NDC 0904-7255-10.

Lot numbers, UPCs & expiration codes

Lot: 25141584, Exp 4/30/2027.

Where it was sold

USA Nationwide

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0736-2026
Classification
Class III
Status
Ongoing
Recall initiated
Jun 30, 2026
FDA report date
Jul 29, 2026
Quantity
2,717 cartons
Recall type
Voluntary: Firm initiated
Recalling firm
Ascend Laboratories, LLC

Original FDA data

Every field from FDA enforcement report D-0736-2026, exactly as published.

Show all FDA fields
City
Bedminster
State
NJ
Status
Ongoing
Country
United States
Event ID
99330
Address
135 Us Highway 202 206 Ste 15
Code information
Lot: 25141584, Exp 4/30/2027.
Postal code
07921-2608
Report date
Jul 29, 2026
Product type
Drugs
Recall number
D-0736-2026
Classification
Class III
Recalling firm
Ascend Laboratories, LLC
Product quantity
2,717 cartons
Reason for recall
Failed Impurities/Degradation Specifications: OOS result was observed during the related substance test analysis with respect to Impurity II, Impurity III and Total impurity testing for 12 Month Long-Term Stability.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Dabigatran etexilate Capsules, 150 mg, 20-count carton (2x10), Rx only, Manufactured by: Alkem Laboratories, Mumbai, INDIA, Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268, NDC 0904-7255-10.
Distribution pattern
USA Nationwide
Recall initiation date
Jun 30, 2026
Initial firm notification
Letter
Center classification date
Aug 4, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0736-2026, published Jul 29, 2026. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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