FDA establishment 3027672712, San Antonio, Texas, United States. Part of Trifluent Pharma LLC's FDA records. Every inspection FDA has posted for the site, with its outcome and cited regulations and its recalls since 2016.
FY2018 to FY2027 to date; 0 classified OAI
A hatched bar is a year that is not over, so its count covers only part of the year.
Inspections citing each reference
| Ended | Product and area | Citations | Classification |
|---|---|---|---|
| Jun 11, 2026 | Drugs · Drug Quality Assurance | 2 cited references
| Voluntary Action Indicated (VAI) |
| Recalled product | Class | Classified |
|---|---|---|
| Tridacaine III / Lidocaine Patch 5%, 15 envelopes containing 1 patch each per pouch, Rx only, Distributed…Drug · D-0181-2027 | Class III | Oct 16, 2026 |
An FEI (FDA Establishment Identifier) names one physical site. Inspections, outcomes and citations come from FDA's Data Dashboard; FDA posts citations only for some inspections. Recalls come from FDA's enforcement reports (iRES), one row per recall even when it covers many lots. A contract site can make products for many companies, so the company shown is the one FDA lists as the site's firm. FDA Data Dashboard, warning letters and enforcement reports
San Antonio, Texas, United States. Part of