Which lot numbers of Silintan capsules are affected?

Every lot and expiration date of Silintan 25-count capsules sold nationwide through 123Herbals.com is covered by the recall.

How do I request a refund for Silintan capsules?

Return the bottle to the retailer or mail it to the 123Herbals Returns Department with proof of purchase or an order number for a full refund.

What symptoms after taking Silintan require immediate medical attention?

Seek care right away for chest pain, shortness of breath, black or bloody stools, severe stomach pain, unexplained bruising, or swelling.

Can I keep using Silintan if I have no side effects?

No. Continued use exposes you to unregulated doses of meloxicam without medical oversight. Discontinue use and speak with your healthcare provider about alternatives.

How should healthcare professionals report adverse events related to Silintan?

Healthcare professionals can report cases to the FDA’s MedWatch program online or by fax at 1-800-FDA-0178, referencing “Silintan capsule recall.”

FDA Recall: Silintan Dietary supplement capsules marketed for Unapproved new drug found to contain undeclared meloxicam

Source: FDA

File Your Claim Now

FDA Recall: Silintan Dietary supplement capsules marketed for Unapproved new drug found to contain undeclared meloxicam

Q: Where was Silintan sold before the recall?

Silintan capsules were distributed exclusively through 123Herbals.com and shipped nationwide within the United States.

Silintan • January 09, 2026

Silintan Dietary Supplement Capsules Recall for Undeclared Meloxicam

Urgent consumer alert — January 7 2026: 123Herbals LLC is recalling every lot of Silintan 25-count capsules after U.S. Food & Drug Administration (FDA) testing found undisclosed meloxicam. Meloxicam is a prescription-only non-steroidal anti-inflammatory drug (NSAID) that can cause life-threatening heart, bleeding, and kidney events when taken without medical supervision.

Why Was Silintan Recalled?

The presence of undeclared meloxicam makes Silintan an unapproved new drug under federal law. Because users are unaware they are ingesting a potent NSAID, they face elevated risks of heart attack, stroke, gastrointestinal bleeding, and acute kidney injury—especially if they also take other NSAIDs, blood thinners, or have pre-existing conditions.

Key Health Risks of Hidden Meloxicam

Heart attack, stroke, or blood clots (risk increases above 15 mg/day)
Gastrointestinal bleeding, ulcers, or intestinal perforation
Acute kidney injury, particularly in older adults or dehydrated users
Dangerous drug interactions with anticoagulants or corticosteroids
Severe allergic or hypersensitivity reactions

Which Silintan Products Are Affected?

All lot numbers and all expiration dates of Silintan 25-count capsules in blue-labeled plastic bottles are included. The product was sold exclusively through 123Herbals.com and shipped to consumers nationwide.

Immediate Steps for Consumers

Stop using Silintan immediately.
Consult a healthcare provider if you have experienced chest pain, shortness of breath, black or bloody stools, severe stomach pain, or unexplained swelling.
Return unopened bottles to the retailer for a refund or dispose of them following local regulations.
Contact 123Herbals at hello@123herbals.com or 1-626-656-3202 (Mon–Fri, 8 a.m.–5 p.m. PT) for recall assistance.
Report adverse reactions to FDA MedWatch via the online form or by calling 1-800-332-1088.

Return & Refund Instructions

Customers who purchased directly from 123Herbals.com can mail the product to:

123Herbals Returns Department
300 West Valley Blvd., P.O. Box 1925
Alhambra, CA 91803

Include proof of purchase or your order number to expedite processing.

Official Images from the Recall

Front view of Silintan dietary supplement bottle — Source: FDA

Back label of Silintan dietary supplement bottle — Source: FDA

Recall Timeline

January 7 2026 — Company announcement submitted to FDA
January 9 2026 — FDA posts public recall notice
Ongoing — 123Herbals emails distributors and consumers

Sources

FDA Recall Notice

Frequently Asked Questions

1. Why was Silintan recalled?: The FDA detected undeclared prescription-strength meloxicam in Silintan capsules, creating serious safety risks and rendering the product an unapproved drug.
2. Which lot numbers of Silintan capsules are affected?: Every lot and every expiration date of Silintan 25-count capsules sold through 123Herbals.com is included in the nationwide recall.
3. How do I request a refund for Silintan capsules?: Return the bottle to the retailer or mail it to the 123Herbals Returns Department with proof of purchase or an order number to receive a full refund.
4. What symptoms after taking Silintan require immediate medical attention?: Seek care right away for chest pain, shortness of breath, black or bloody stools, severe stomach pain, unexplained bruising, or swelling.
5. Can I keep using Silintan if I have no side effects?: No. Continued use exposes you to unregulated doses of meloxicam without physician oversight. Discontinue use and discuss safer options with your healthcare provider.
6. How should healthcare professionals report adverse events related to Silintan?: Providers can report cases to the FDA’s MedWatch program online or by fax at 1-800-FDA-0178, referencing “Silintan capsule recall.”
7. Where was Silintan sold before the recall?: The product was distributed exclusively online at 123Herbals.com and shipped to customers across the United States.