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FDA · Drug recall

Tridacaine III / Lidocaine Patch 5%…

Recall started · FDA enforcement report Nov. 4, 2026 · On this site since Nov. 11, 2026 Not Yet Classified

Reason
Labeling: Incorrect or Missing Lot and/or Exp Date. Incorrect expiration date printed on the label.
Status
Ongoing
Distribution
US

This box checks this one record only. Other recalls of the same product or company are on the brand page.

Enforcement report date
Nov. 4, 2026
Risk class
Not Yet Classified
Status
Ongoing (FDA's definition: a recall which is currently in progress; as in openFDA's data of Nov. 10, 2026)
Filed by
Trifluent Pharma LLC
Product
Tridacaine III / Lidocaine Patch 5%, 15 envelopes containing 1 patch each per pouch, Rx only, Distributed by: Trifluent Pharma San Antonio, TX 78213, NDC 73352-835-15.
Reason
Labeling: Incorrect or Missing Lot and/or Exp Date. Incorrect expiration date printed on the label.
Distribution pattern
US
Quantity
68 pouches
Codes and lots
Lot #: L2606225A, Exp. Date 06/22/2029.
Recall started
Oct. 16, 2026
Voluntary or mandated
Voluntary: Firm initiated

What the record says about this drug

A simplified drawing of a vial, following the words of FDA's record. It shows the reason the record gives, not a photograph of the product.

Four steps: a container, the reason the record gives, the record's wordsA simplified drawing of a drug's container with a mark for the reason the record gives. Left, for comparison: the same drawing without what the record names. Right: this record.1 The product: Tridacaine III / Lidocaine Patch 5%, 15…2 The record names a labeling problem3 What the record says4 What the record listsFOR COMPARISONthe same drawing, withoutwhat the record namesTHIS RECORDwhat the record names,step by stepIncorrect or Missing Lot and/or Exp Date

“Labeling: Incorrect or Missing Lot and/or Exp Date. Incorrect expiration date printed on the label.”Tridacaine III / Lidocaine Patch 5%, 15 envelopes containing 1 patch each per pouch, Rx only, Distributed by: Trifluent Pharma San Antonio, TX 78213, NDC 73352-835-15., FDA enforcement report, 2026-11-04. The caption is the record's own words.

A generic vial, not the product. The mark follows the record's own words (a question mark, where used, stands for a lack of assurance the record names, not for anything found).

If the drawing and the record's words differ, the words govern. A drawing is chosen by rules and an AI reading of the record and can miss what it means; report one with the form below.

This recall among the others

  • FDA's enforcement report came 19 days after the firm started the recall. For half of the 310 FDA drug recall events reported in 2026 so far with a start date, it took 23 days or fewer (by year).

Counted from the agency records on this site, as on Statistics: a recall event once, by its first notice.

What should I do? Medicine recall: what to do · How to read this record

Source: FDA · Drug enforcement report, recall number (no number given yet). See this record in openFDA (FDA's own data service; it answers in JSON). The agency record governs; check it and the company before acting.

Cite this record
FDA recall record (no number given yet), Nov. 4, 2026. "Tridacaine III / Lidocaine Patch 5%." PlainRecords, https://plainrecords.com/recall/drug/n-a-100178-e1bd3f/ (on this site since Nov. 11, 2026; as of the day it was built).

At each build a sample of records from each source is compared with the agency's published file and the page; every correction is public. Drawings are chosen by software that reads the record. Built daily. How we check · Corrections

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