Fesoterodine Fumarate, Extended-release Tablets, 8 mg, 30 Tablets, Rx only, Manufactured by: Alembic Pharmaceuticals Limited, Panelav 389350, Gujarat, India, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, NDC 62332-176-30
USFesoterodine Fumarate, Extended-release Tablets, 8 mg, 30 Tablets, Rx only, Manufactured by: Alembic Pharmaceuticals Limited, Panelav 389350, Gujarat, India, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, NDC 62332-176-30
Recalling Firm: Alembic Pharmaceuticals Limited
Motif du rappel / Danger
TranslatedFailed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.
Description du produit & Identification
TranslatedFesoterodine Fumarate, Extended-release Tablets, 8 mg, 30 Tablets, Rx only, Manufactured by: Alembic Pharmaceuticals Limited, Panelav 389350, Gujarat, India, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, NDC 62332-176-30
Additional Source Details
| Field | Value |
|---|---|
| City | Panchmahal |
| Openfda › Upc › 1 | 0362332176304 |
| Openfda › Upc › 2 | 0362332175307 |
| Openfda › Unii | EOS72165S7 |
| Openfda › Route | ORAL |
| Openfda › Rxcui › 1 | 810071 |
| Openfda › Rxcui › 2 | 810077 |
| Openfda › Spl id | 2fc9ba3f-2336-45b8-9020-bffc1298a6e0 |
| Openfda › Brand name | FESOTERODINE FUMARATE |
| Openfda › Spl set id | 299db62d-9658-4796-b449-657fa859c5cd |
| Openfda › Package ndc › 1 | 62332-175-30 |
| Openfda › Package ndc › 2 | 62332-175-90 |
| Openfda › Package ndc › 3 | 62332-175-91 |
| Openfda › Package ndc › 4 | 62332-175-10 |
| Openfda › Package ndc › 5 | 62332-176-30 |
| Openfda › Package ndc › 6 | 62332-176-90 |
| Openfda › Package ndc › 7 | 62332-176-91 |
| Openfda › Package ndc › 8 | 62332-176-10 |
| Openfda › Package ndc › 9 | 2405003360 |
| Openfda › Product ndc › 1 | 62332-175 |
| Openfda › Product ndc › 2 | 62332-176 |
| Openfda › Generic name | FESOTERODINE FUMARATE |
| Openfda › Product type | HUMAN PRESCRIPTION DRUG |
| Openfda › Substance name | FESOTERODINE FUMARATE |
| Openfda › Manufacturer name | Alembic Pharmaceuticals Inc. |
| Openfda › Application number | ANDA204973 |
| Openfda › Is original packager | true |
| Event id | 98119 |
| Address 1 | Formulation Division, Village Panelav, P.O. Tajpura, Near Baska, Taluka Halol |
| Code info | Lot# 2405003360, Exp Date: Jan 31, 2026 |
| Postal code | N/A |
| Report date | 20260114 |
| Product type | Drugs |
| Reason for recall | Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20251216 |
| Center classification date | 20260102 |
Consumer Action Protocol: What You Should Do Immediately
Safety StepsInspect the NDC code, batch number, or control number on your medicine bottle or blister packaging to confirm whether your unit is included.
Do not abruptly stop critical prescribed medication without physician advice. Contact your dispensing pharmacist immediately for a safe alternative.
Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.
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 GuideQ1:What should I do immediately if I own or bought Fesoterodine Fumarate, Extended-release Tablets, 8 mg, 30 Tablets, Rx only, Manufactured by: Alembic Pharmaceuticals...?
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 responsableAlembic Pharmaceuticals Limited
- StatusOngoing
- Niveau de risqueClass III
- DistributionUS Nationwide and PR.
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🚨 SAFETY ALERT: Alembic Pharmaceuticals Limited - Fesoterodine Fumarate, Extended-release Tablets, 8 mg, 30 Tablets, Rx only, Manufactured by: Alembic Pharmaceuticals Limited, Panelav 389350, Gujarat, India, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, NDC 62332-176-30 Check if your household is affected: https://therecallfile.com/fr/recalls/fesoterodine-fumarate-extended-release-tablets-8-mg-30-tablets-rx-only/FDA-D-0248-2026
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