Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Low RiskFDA Drug
Medications & Supplements/Prescription Drugs

Strides Pharma Inc.: Tacrolimus Capsules Recalled for Failing Moisture Limits

Agency Publication Date: December 30, 2020
Share:
Sign in to monitor this recall

Summary

Strides Pharma Inc. has voluntarily recalled 960 bottles of Tacrolimus Capsules USP (1mg), a prescription medication used to prevent organ rejection. This recall was initiated because the product failed to meet moisture limit specifications during stability testing. Consumers should contact their healthcare provider or pharmacist for guidance, as medication that does not meet quality standards may not perform as intended.

Risk

The failure to meet moisture limits can affect the stability and chemical integrity of the medication over time, potentially leading to reduced effectiveness of the drug.

What You Should Do

  1. Identify your medication by checking the bottle label for 'TACROLIMUS CAPSULES, USP 1mg' in 100-count bottles with NDC 64380-721-06.
  2. Check the bottle for Lot number 7242728A with an expiration date of June 2023.
  3. If you have the affected medication, contact your healthcare provider or pharmacist immediately to discuss an alternative supply and ensure your treatment is not interrupted.
  4. Return any unused capsules from the affected lot to your pharmacy for a refund.
  5. Contact Strides Pharma Inc. at their East Brunswick, NJ office for further instructions regarding this recall.
  6. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Return unused product for a refund.

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: TACROLIMUS CAPSULES, USP 1mg (100 Capsules)
Model:
NDC 64380-721-06
Recall #: D-0180-2021
Lot Numbers:
7242728A (Exp June 2023)
Date Ranges: June 2023

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 87027
Status: Resolved
Manufacturer: Strides Pharma Inc.
Sold By: pharmacies
Manufactured In: India, United States
Units Affected: 960 bottles
Distributed To: Pennsylvania

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.