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

Buspirone and Lisinopril Tablets Recalled for Potential Foreign Tablet Presence

Agency Publication Date: November 21, 2023
Share:
Sign in to monitor this recall

Summary

NCS Healthcare of Kentucky Inc is recalling 1,356 blister cards of Buspirone Hydrochloride (10 mg) and Lisinopril (20 mg) tablets because they may contain stray tablets of a different medication, Amlodipine Besylate (10 mg). The products were distributed nationwide in the USA. No incidents or injuries have been reported to date. Consumers should consult their healthcare provider or pharmacist if they have concerns about their medication.

Risk

Taking an unintended medication like Amlodipine Besylate instead of your prescribed dose could lead to unexpected side effects or cause your actual condition to go untreated.

What You Should Do

  1. This recall affects Buspirone Hydrochloride (10 mg) and Lisinopril (20 mg) prescription tablets sold in 15-count and 30-count blister cards.
  2. Check your blister cards for lot number 7718-3008 (Expiration 08/31/2024) for Buspirone or lot number 8255-3012 (Expiration 08/31/2024) for Lisinopril.
  3. Verify the NDC numbers printed on the packaging: 0615-7718-05, 0615-7718-39, or 0615-8255-39.
  4. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  5. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for more information.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Buspirone Hydrochloride Tabs USP 10 mg
Variants: 15-count blister card, 30-count blister card, 10 mg
Lot Numbers:
7718-3008 (Exp 08/31/2024)
NDC:
0615-7718-05
0615-7718-39

Mfd By Pliva HRVATSKA for Teva USA, PKG by Vangard Glasgow, KY 42141.

Product: Lisinopril Tablets USP 20 mg
Variants: 15-count blister card, 30-count blister card, 20 mg
Lot Numbers:
8255-3012 (Exp 08/31/2024)
NDC:
0615-7718-05
0615-8255-39

Mfd By Lupin, PKG by Vangard Glasgow, KY 42141.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93336
Status: Resolved
Manufacturer: NCS Healthcare of Kentucky Inc
Sold By: Pharmacies
Manufactured In: United States
Units Affected: 2 products (1,344 cards; 12 cards)
Distributed To: Nationwide

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.