Bromfenac Ophthalmic Solution 0.07%, 3 ml, Rx only, Sterile, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, Made in India, Manufactured by: Alembic Pharmaceuticals Limited, Karakhadi- 391 450, Gujarat, India NDC 62332-583-03.
USBromfenac Ophthalmic Solution 0.07%, 3 ml, Rx only, Sterile, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, Made in India, Manufactured by: Alembic Pharmaceuticals Limited, Karakhadi- 391 450, Gujarat, India NDC 62332-583-03.
Recalling Firm: ALEMBIC PHARMACEUTICALS, INC.
Grund für den Rückruf / Gefahr
TranslatedFailed Impurities/Degradation Specifications: out of specification at the time of testing i.e. 20th month stability testing.
Produktbeschreibung & Identifikation
TranslatedBromfenac Ophthalmic Solution 0.07%, 3 ml, Rx only, Sterile, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, Made in India, Manufactured by: Alembic Pharmaceuticals Limited, Karakhadi- 391 450, Gujarat, India NDC 62332-583-03.
Additional Source Details
| Field | Value |
|---|---|
| City | Bedminster |
| State | NJ |
| Openfda › Unii | 8ECV571Y37 |
| Openfda › Route | OPHTHALMIC |
| Openfda › Rxcui | 1375917 |
| Openfda › Spl id | e680d513-20c9-4595-a293-d3f57d24f428 |
| Openfda › Brand name | BROMFENAC SODIUM |
| Openfda › Spl set id | f6911061-d00e-466d-b623-f81730f38f98 |
| Openfda › Package ndc | 62332-583-03 |
| Openfda › Product ndc | 62332-583 |
| Openfda › Generic name | BROMFENAC SODIUM |
| Openfda › Product type | HUMAN PRESCRIPTION DRUG |
| Openfda › Substance name | BROMFENAC SODIUM |
| Openfda › Manufacturer name | Alembic Pharmaceuticals Inc. |
| Openfda › Application number | ANDA214340 |
| Openfda › Is original packager | true |
| Event id | 98647 |
| Address 1 | 550 Hills Dr Ste 104b |
| Code info | Lot # 7240184, 7240185, 7240186, 7240187, Exp Date: 3/31/2026; Lot # 7240278, Exp Date: 5/31/2026. |
| Postal code | 07921-1537 |
| Report date | 20260408 |
| Product type | Drugs |
| Reason for recall | Failed Impurities/Degradation Specifications: out of specification at the time of testing i.e. 20th month stability testing. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260318 |
| Initial firm notification | Letter |
| Center classification date | 20260331 |
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 Bromfenac Ophthalmic Solution 0.07%, 3 ml, Rx only, Sterile, Manufactured for: Alembic Pharmaceuticals, Inc., Bedmins...?
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 UnternehmenALEMBIC PHARMACEUTICALS, INC.
- StatusOngoing
- RisikostufeClass II
- DistributionNationwide in the USA
📢 Warnung teilen
Alert family and friends to keep them safe. Copy this quick alert message:
🚨 SAFETY ALERT: ALEMBIC PHARMACEUTICALS, INC. - Bromfenac Ophthalmic Solution 0.07%, 3 ml, Rx only, Sterile, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, Made in India, Manufactured by: Alembic Pharmaceuticals Limited, Karakhadi- 391 450, Gujarat, India NDC 62332-583-03. Check if your household is affected: https://therecallfile.com/de/recalls/bromfenac-ophthalmic-solution-0-07-3-ml-rx-only-sterile-manufactured-f/FDA-98647
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