Accueil/Tous les Rappels/FDA-D-0676-2026
FDA DrugsClass II

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

Publié le: 8 juillet 2026ID du rappel: D-0676-2026Catégorie: Médicaments & SantéPays: États-Unis
US
PharmaceuticalFDA DrugsUSUS

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

Recalling Firm: Cipla USA, Inc.

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Traduire l’alerteTranslate notice text, hazard warnings, and descriptions into any supported language.

Motif du rappel / Danger

cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).

Description du produit & Identification

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

Additional Source Details

FieldValue
CityWarren
StateNJ
Openfda › Unii1K860WSG25
Openfda › RouteORAL
Openfda › Rxcui › 1432400
Openfda › Rxcui › 2432401
Openfda › Rxcui › 3432402
Openfda › Spl id383a7dc8-b195-4868-8774-f16a5558771e
Openfda › Brand nameCINACALCET
Openfda › Spl set id02b8c11b-99e8-4039-b6fa-a9c38d2f48fa
Openfda › Package ndc › 169097-410-02
Openfda › Package ndc › 269097-411-02
Openfda › Package ndc › 369097-412-02
Openfda › Product ndc › 169097-410
Openfda › Product ndc › 269097-411
Openfda › Product ndc › 369097-412
Openfda › Generic nameCINACALCET
Openfda › Product typeHUMAN PRESCRIPTION DRUG
Openfda › Substance nameCINACALCET HYDROCHLORIDE
Openfda › Manufacturer nameCipla USA Inc.
Openfda › Application numberANDA208915
Openfda › Is original packagertrue
Event id99350
Address 110 Independence Blvd
Address 2N/A
Code infoLot #: 5PB0563, Exp 4/30/2027
Postal code07059-2730
Report date20260708
Product typeDrugs
Product quantityN/A
Reason for recallcGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260629
Initial firm notificationLetter
Center classification date20260709

Consumer Action Protocol: What You Should Do Immediately

Safety Steps
1Verify Product Identifiers

Inspect the NDC code, batch number, or control number on your medicine bottle or blister packaging to confirm whether your unit is included.

2Isolate & Discontinue Use

Do not abruptly stop critical prescribed medication without physician advice. Contact your dispensing pharmacist immediately for a safe alternative.

3Claim Free Statutory Remedy

Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.

4Report Adverse Incidents

If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (FDA Drugs).

Your Legal Rights as a Consumer

Recalls are legally binding corrective safety actions overseen by statutory government bodies. Recalling entities are legally prohibited from charging consumers for official safety remedies. If a retailer or dealership refuses your recall remedy, notify the issuing regulatory agency immediately.

Frequently Asked Questions About This Recall

FAQ Guide

Q1:What should I do immediately if I own or bought Cinacalcet Hydrochloride Tablets, 90 mg, 30-count bottle, Rx Only, Manufactured by: Cipla Ltd., MIDC, Patalganga, Ind...?

Check the lot number and NDC on your prescription label. For essential medications, consult your doctor or dispensing pharmacist immediately before abruptly stopping your dose.

Q2:Can I get a full refund or free repair for this recall?

Yes. Recalling manufacturers and retail merchants are required under consumer protection regulations to offer a statutory remedy—typically a full refund, certified repair kit, or replacement unit.

Q3:Do I need my original sales receipt to claim a remedy or refund?

In most recall cases, no receipt is required. Because safety recalls are matters of public health and statutory compliance, retailers and manufacturers routinely issue refunds, store credit, or replacement kits upon presentation of the affected product or lot code.

Q4:Where can I verify official information for this safety alert?

This safety alert is aggregated directly from official regulatory agency records (FDA Drugs). You can click the 'Official Agency Alert' link on this page to view the primary government notice and contact the manufacturer directly.

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Aperçu

  • Entreprise responsableCipla USA, Inc.
  • StatusOngoing
  • Niveau de risqueClass II
  • DistributionUSA Nationwide
Recall Hazard Severity
High Alert (Class I)
Alerte officielle de l’agence

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🚨 SAFETY ALERT: Cipla USA, Inc. - 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

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https://therecallfile.com/fr/recalls/cinacalcet-hydrochloride-tablets-90-mg-30-count-bottle-rx-only-manufac/FDA-D-0676-2026
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