FDA · Drugs ·
Cinacalcet Hydrochloride Tablets recall
Cipla USA, Inc. recalled Cinacalcet Hydrochloride Tablets on July 8, 2026 because of cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI). It was sold nationwide.
Why it was recalled
cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).
What's recalled
Cinacalcet Hydrochloride Tablets, 30 mg, 30-count bottle, Rx Only, Manufactured by: Cipla Ltd., MIDC, Patalganga, India; Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059, NDC 69097-410-02
Quantity: 31,824 bottles
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Cipla USA, Inc., Warren, NJ
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
USA Nationwide - Status
- Ongoing
- Recall number
- D-0661-2026
- Source
- U.S. Food and Drug Administration
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