FDA recall,
Trifluent Pharma Tridacaine III Lidocaine Patch 5%
The lidocaine patch has incorrect or missing lot and expiration dates.
Summary by Recall Canary from the FDA notice
What happened
Trifluent Pharma LLC of San Antonio, Texas, is voluntarily recalling Tridacaine III / Lidocaine Patch 5%, a prescription product distributed in pouches containing 15 envelopes with 1 patch each, because the label has an incorrect expiration date printed on it. The recall involves 68 pouches and was initiated by the company on October 16, 2026.
The recall was added to the FDA's Enforcement Report on October 28, 2026, and is in the weekly enforcement report dated November 4, 2026. Customers were told by telephone.
What to do
The FDA notice gives no instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is yours affected?
Match the NDC and lot code listed under your product.
An NDC (National Drug Code) is usually printed on the drug's label.
Tridacaine III Lidocaine Patch 5%
- NDC
- 73352-835-15
- Lot code
- L2606225A
Recall details
- Posted by FDA
- Recall began
- Status
- Open
- Weekly archive
- Listed the week of Oct 26, 2026
- Sold in
US
- Recalled by
- Trifluent Pharma LLCSan Antonio, Texas
- Hazard
- Labeling error
- Risk
Not yet rated by FDA
- FDA event number
- 100178
- Quantity recalled
- 68 pouches
- Recall type
- Voluntary: Firm initiated
- How the company first told customers
- Telephone
All recalls from Trifluent Pharma LLC
Timeline
FDA's Enforcement Report is its public list of recalls; FDA posts a recall by adding it there.
Trifluent Pharma began the recall
FDA posted the recall to its Enforcement Report
Added to Recall Canary
Summary updated
