Severity
Low
LowClass IIIOngoing
FDA Drug recall · Reported February 18, 2026
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.
Tablets/Capsules Imprinted with Wrong ID
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
Unichem Pharmaceuticals USA Inc. recalled Doxazosin Tablets, USP, 4 mg, 1000 tablets per bottle, Rx only, distributed by Unichem Ph… - a low-severity action.
Doxazosin Tablets, USP, 4 mg, 1000 tablets per bottle, Rx only, distributed by Unichem Ph… was recalled by Unichem Pharmaceuticals USA Inc. in February 18, 2026. Reason: Tablets/Capsules Imprinted with Wrong ID. Check the official notice for the remedy. Verify recall #D-0306-2026 with the FDA Drug before acting.
The recall
Unichem Pharmaceuticals USA Inc. issued this low-severity FDA Drug recall-Tablets/Capsules Imprinted with Wrong ID.
- Low
- severity level
- Class III
- classification
- February 18, 2026
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0306-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0306-2026) was formally reported on February 18, 2026, with the manufacturer initiating the action on January 21, 2026. It is classified under Low severity (Class III), with a current status of Ongoing. Unichem Pharmaceuticals USA Inc. is listed as the recalling firm, operating out of East Brunswick, NJ. Federal records list the affected scope as 60,000 tablets.
The documented reason for this recall is: Tablets/Capsules Imprinted with Wrong ID Distribution data in the federal record shows the product reached: Nationwide. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
60,000 tablets
Related Recalls
6
0 from same agency
Product description
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.
Reason for recall
Tablets/Capsules Imprinted with Wrong ID
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Ongoing |
| Recall number | D-0306-2026 |
| Date reported | February 18, 2026 |
| Date initiated | January 21, 2026 |
| Recalling firm | Unichem Pharmaceuticals USA Inc. |
| Firm location | East Brunswick, NJ |
| Affected scope | 60,000 tablets |
| Distribution | Nationwide |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-0306-2026) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Unichem Pharmaceuticals USA Inc.. Units affected: 60,000 tablets.
Why was this product recalled? ▼
Tablets/Capsules Imprinted with Wrong ID
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 18, 2026. Severity: Low. Recall number: D-0306-2026.
Where was the recalled product distributed? ▼
Distribution: Nationwide.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0306-2026) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported February 18, 2026. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.