Cinacalcet Hydrochloride Tablets — Class II drug recall D-0676-2026
Ongoing recall by Cipla USA, Inc., reported 2026-07-08, distributed nationwide. cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).
| Recall number | D-0676-2026 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cipla USA, Inc., Warren, NJ, United States |
| Recall initiated | 2026-06-29 |
| Classified | 2026-07-09 |
| Reported by FDA | 2026-07-08 |
| Distributed | Nationwide (US) |
| Reason classes | cgmp |
| NDC | 69097-0410, 69097-0410-02, 69097-0411, 69097-0411-02, 69097-0412, 69097-0412-02 |
| Lot numbers | 5PB0563 |
| Expiration dates | 2027-04-30 |
Product
Cinacalcet Hydrochloride Tablets, 90 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 69097-412-02
Reason for recall
cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0676-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.