Startseite/Alle Rückrufe/FDA-D-0341-2026
FDA DrugsClass II

Amantadine HCl, Capsules, UPS, 100 mg, 50 Capsules (5 x 10) unit dose, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478, www.avkare.com, NDC 50268-069-15.

Veröffentlicht: 4. März 2026Rückruf-ID: D-0341-2026Kategorie: Arzneimittel & MedikamenteLand: Vereinigte Staaten
US
PharmaceuticalFDA DrugsUSUS

Amantadine HCl, Capsules, UPS, 100 mg, 50 Capsules (5 x 10) unit dose, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478, www.avkare.com, NDC 50268-069-15.

Recalling Firm: AvKARE

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

Grund für den Rückruf / Gefahr

Failed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution.

Produktbeschreibung & Identifikation

Amantadine HCl, Capsules, UPS, 100 mg, 50 Capsules (5 x 10) unit dose, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478, www.avkare.com, NDC 50268-069-15.

Additional Source Details

FieldValue
CityPulaski
StateTN
Openfda › UniiM6Q1EO9TD0
Openfda › RouteORAL
Openfda › Rxcui849389
Openfda › Spl id38566e1f-b7b1-540f-e063-6394a90a2760
Openfda › Brand nameAMANTADINE HCL
Openfda › Spl set id461e6444-189e-62ed-6c61-1c36a04459c6
Openfda › Package ndc › 150268-069-11
Openfda › Package ndc › 250268-069-15
Openfda › Product ndc50268-069
Openfda › Generic nameAMANTADINE HYDROCHLORIDE
Openfda › Product typeHUMAN PRESCRIPTION DRUG
Openfda › Substance nameAMANTADINE HYDROCHLORIDE
Openfda › Manufacturer nameAvPAK
Openfda › Application numberANDA078720
Openfda › Original packager product ndc69452-142
Event id98449
Address 1615 N 1st St
Address 2N/A
Code infoLot # 49261, Exp: 04/30/27
Postal code38478-2403
Report date20260304
Product typeDrugs
Product quantityN/A
Reason for recallFailed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260213
Initial firm notificationLetter
Center classification date20260223

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 Amantadine HCl, Capsules, UPS, 100 mg, 50 Capsules (5 x 10) unit dose, Rx Only, Manufactured for: AvKARE, Pulaski, TN...?

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 UnternehmenAvKARE
  • StatusOngoing
  • RisikostufeClass II
  • DistributionNationwide in the USA.
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: AvKARE - Amantadine HCl, Capsules, UPS, 100 mg, 50 Capsules (5 x 10) unit dose, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478, www.avkare.com, NDC 50268-069-15.

Check if your household is affected:
https://therecallfile.com/de/recalls/amantadine-hcl-capsules-ups-100-mg-50-capsules-5-x-10-unit-dose-rx-onl/FDA-D-0341-2026
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