Startseite/Alle Rückrufe/FDA-D-0391-2026
FDA DrugsClass III

Pitavastatin Tablets, 2 mg, packaged in 90-count bottles, Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Annora Pharma Pvt. LTd., Sengareddy - 502313, Telengana, India, NDC 72603-479-01.

Veröffentlicht: 25. März 2026Rückruf-ID: D-0391-2026Kategorie: Arzneimittel & MedikamenteLand: Vereinigte Staaten
US
PharmaceuticalFDA DrugsUSUS

Pitavastatin Tablets, 2 mg, packaged in 90-count bottles, Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Annora Pharma Pvt. LTd., Sengareddy - 502313, Telengana, India, NDC 72603-479-01.

Recalling Firm: Annora Pharma Private Limited

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Mitteilung übersetzenTranslate notice text, hazard warnings, and descriptions into any supported language.

Grund für den Rückruf / Gefahr

Presence of foreign tablets/capsules: one Pitavastatin tablet 1mg found in bottle of Pitavastatin tablets 2mg

Produktbeschreibung & Identifikation

Pitavastatin Tablets, 2 mg, packaged in 90-count bottles, Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Annora Pharma Pvt. LTd., Sengareddy - 502313, Telengana, India, NDC 72603-479-01.

Additional Source Details

FieldValue
CityHyderabad
StateN/A
Openfda › UniiIYD54XEG3W
Openfda › RouteORAL
Openfda › Rxcui › 1861648
Openfda › Rxcui › 2861652
Openfda › Spl id27e1ba97-23bf-fc12-e063-6394a90a1699
Openfda › Brand namePITAVASTATIN CALCIUM
Openfda › Spl set id98e3f1df-5b38-4169-a340-adb145eac459
Openfda › Package ndc › 172603-479-01
Openfda › Package ndc › 272603-480-01
Openfda › Product ndc › 172603-479
Openfda › Product ndc › 272603-480
Openfda › Generic namePITAVASTATIN CALCIUM
Openfda › Product typeHUMAN PRESCRIPTION DRUG
Openfda › Substance namePITAVASTATIN CALCIUM
Openfda › Manufacturer nameNorthStar RxLLC
Openfda › Application numberANDA205977
Openfda › Is original packagertrue
Event id98543
Address 1Sy. No.261, Plot No. 13 And 14, Annaram Village, Gummadidal Mandal
Address 2Jinnaram Mandal, Sangareddy District, Medak
Code infoLot #: A252487, Exp 05/31/2027
Postal codeN/A
Report date20260325
Product typeDrugs
Product quantity770 bottles
Reason for recallPresence of foreign tablets/capsules: one Pitavastatin tablet 1mg found in bottle of Pitavastatin tablets 2mg
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260203
Initial firm notificationLetter
Center classification date20260316

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 Pitavastatin Tablets, 2 mg, packaged in 90-count bottles, Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38...?

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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Übersicht

  • Rückrufendes UnternehmenAnnora Pharma Private Limited
  • StatusOngoing
  • RisikostufeClass III
  • DistributionTN
Recall Hazard Severity
High Alert (Class I)
Offizielle Behördenwarnung

📢 Warnung teilen

Alert family and friends to keep them safe. Copy this quick alert message:

🚨 SAFETY ALERT: Annora Pharma Private Limited - Pitavastatin Tablets, 2 mg, packaged in 90-count bottles, Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Annora Pharma Pvt. LTd., Sengareddy - 502313, Telengana, India, NDC 72603-479-01.

Check if your household is affected:
https://therecallfile.com/de/recalls/pitavastatin-tablets-2-mg-packaged-in-90-count-bottles-rx-only-manufac/FDA-D-0391-2026
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