Doxazosin Tablets, USP, 4 mg, 1000 tablets per bottle, Rx only, distributed by Unichem Pharmaceuticals (USA), Inc., 1 Tower Center Boulevard, Suite 2200, East Brunswick, NJ 08816 USA, manufactured by Unichem Laboratories Limited, Plot Number 15 to 18, Pilerne Industrial Estate, Pilerne, Bardez, Goa (India) 403511, NDC 29300-353-10.
USDoxazosin Tablets, USP, 4 mg, 1000 tablets per bottle, Rx only, distributed by Unichem Pharmaceuticals (USA), Inc., 1 Tower Center Boulevard, Suite 2200, East Brunswick, NJ 08816 USA, manufactured by Unichem Laboratories Limited, Plot Number 15 to 18, Pilerne Industrial Estate, Pilerne, Bardez, Goa (India) 403511, NDC 29300-353-10.
Recalling Firm: Unichem Pharmaceuticals USA Inc.
Grund für den Rückruf / Gefahr
TranslatedTablets/Capsules Imprinted with Wrong ID
Produktbeschreibung & Identifikation
TranslatedDoxazosin Tablets, USP, 4 mg, 1000 tablets per bottle, Rx only, distributed by Unichem Pharmaceuticals (USA), Inc., 1 Tower Center Boulevard, Suite 2200, East Brunswick, NJ 08816 USA, manufactured by Unichem Laboratories Limited, Plot Number 15 to 18, Pilerne Industrial Estate, Pilerne, Bardez, Goa (India) 403511, NDC 29300-353-10.
Additional Source Details
| Field | Value |
|---|---|
| City | East Brunswick |
| State | NJ |
| Openfda › Unii | 86P6PQK0MU |
| Openfda › Route | ORAL |
| Openfda › Rxcui › 1 | 197625 |
| Openfda › Rxcui › 2 | 197626 |
| Openfda › Rxcui › 3 | 197627 |
| Openfda › Rxcui › 4 | 197628 |
| Openfda › Spl id | e2406e8e-68c2-49dc-9e15-6170f3fffa03 |
| Openfda › Brand name | DOXAZOSIN MESYLATE |
| Openfda › Spl set id | 44bfe5d7-a56a-46f1-8ef3-ad386ab35f0f |
| Openfda › Package ndc › 1 | 29300-351-13 |
| Openfda › Package ndc › 2 | 29300-351-01 |
| Openfda › Package ndc › 3 | 29300-351-10 |
| Openfda › Package ndc › 4 | 29300-352-13 |
| Openfda › Package ndc › 5 | 29300-352-01 |
| Openfda › Package ndc › 6 | 29300-352-10 |
| Openfda › Package ndc › 7 | 29300-353-13 |
| Openfda › Package ndc › 8 | 29300-353-01 |
| Openfda › Package ndc › 9 | 29300-353-10 |
| Openfda › Package ndc › 10 | 29300-354-13 |
| Openfda › Package ndc › 11 | 29300-354-01 |
| Openfda › Package ndc › 12 | 29300-354-10 |
| Openfda › Product ndc › 1 | 29300-351 |
| Openfda › Product ndc › 2 | 29300-352 |
| Openfda › Product ndc › 3 | 29300-353 |
| Openfda › Product ndc › 4 | 29300-354 |
| Openfda › Generic name | DOXAZOSIN MESYLATE |
| Openfda › Product type | HUMAN PRESCRIPTION DRUG |
| Openfda › Substance name | DOXAZOSIN MESYLATE |
| Openfda › Manufacturer name | Unichem Pharmaceuticals (USA), Inc. |
| Openfda › Application number | ANDA212329 |
| Openfda › Is original packager | true |
| Event id | 98321 |
| Address 1 | 1 Tower Center Blvd Ste 2200 |
| Address 2 | N/A |
| Code info | Lot # GDSH25006, Exp Date: 08/2027 |
| Postal code | 08816-1145 |
| Report date | 20260218 |
| Product type | Drugs |
| Product quantity | 60,000 tablets |
| Reason for recall | Tablets/Capsules Imprinted with Wrong ID |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260121 |
| Initial firm notification | Letter |
| Center classification date | 20260211 |
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 Doxazosin Tablets, USP, 4 mg, 1000 tablets per bottle, Rx only, distributed by Unichem Pharmaceuticals (USA), Inc., 1...?
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 UnternehmenUnichem Pharmaceuticals USA Inc.
- StatusOngoing
- RisikostufeClass III
- DistributionNationwide
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🚨 SAFETY ALERT: Unichem Pharmaceuticals USA Inc. - Doxazosin Tablets, USP, 4 mg, 1000 tablets per bottle, Rx only, distributed by Unichem Pharmaceuticals (USA), Inc., 1 Tower Center Boulevard, Suite 2200, East Brunswick, NJ 08816 USA, manufactured by Unichem Laboratories Limited, Plot Number 15 to 18, Pilerne Industrial Estate, Pilerne, Bardez, Goa (India) 403511, NDC 29300-353-10. Check if your household is affected: https://therecallfile.com/de/recalls/doxazosin-tablets-usp-4-mg-1000-tablets-per-bottle-rx-only-distributed/FDA-D-0306-2026
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