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Class III · Lower riskRecall completed

Buspirone Hydrochloride

Unlikely to cause harm — often a labeling or packaging issue.

Does this affect you?
Check your lot numberLot#: a) [redacted-phone], Exp 08/31/2024; b) [redacted-phone], Exp 08/31/2024
Where it was soldNationwide USA
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Presence of Foreign Tablets: Potential of stray tablet(s) of Amlodipine Besylate 10 mg Tablet within the recalled lots

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byNCS HealthCare of KY, LLC dba Vangard Labs
Brand nameBUSPIRONE HYDROCHLORIDE, LISINOPRIL
Generic nameBUSPIRONE HYDROCHLORIDE, LISINOPRIL
Active ingredient(s)BUSPIRONE HYDROCHLORIDE, LISINOPRIL
Distributed by / forNCS Healthcare of Kentucky Inc
NDC0615-7718-05
Show the full FDA record
Full product labelLisinopril Tablets USP 20 mg, packaged in a) 15-count blister card (NDC 0615-7718-05), b) 30-count blister card (NDC 0615-8255-39), Rx only, Mfd By Lupin, PKG by Vangard Glasgow, KY 42141.
Recalling firmNCS Healthcare of Kentucky Inc
DistributionNationwide USA
Quantity12 cards
Recall initiated2023-10-27
Report date2023-11-29
Recall completed2024-07-14
Recall numberD-0114-2024
ClassificationClass III
FDA statusTerminated
Origin on fileGlasgow KY United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.