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Class II · ModerateActive recall

Tridergel

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot #: BL3435, Exp. 11/06/26
Where it was soldNationwide in the USA
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

CGMP Deviations: product manufactured in the same facility under the same conditions as the product found to be contaminated

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byTrifluent Pharma LLC
Brand nameTRIDERGEL
Generic nameBENZALKONIUM CHLORIDE
Active ingredient(s)BENZALKONIUM CHLORIDE
Distributed by / forTrifluent Pharma, LLC. San Antonio, TX 78213
NDC73352-520-01
Show the full FDA record
Full product labelTRIFLUENT PHARMA TRIDERGEL Wound Care Gel, (Benzalkonium Chloride 0.1%), 1.0 fl oz, (29.6 mL) bottle with long pointy cap, Manufactured for: Trifluent Pharma, LLC. San Antonio, TX 78213. NDC 73352-520-01.
Recalling firmBlaine Labs Inc
DistributionNationwide in the USA
Quantity519 - 1 oz bottles
Recall initiated2026-04-08
Report date2026-07-08
Recall completed—
Recall numberD-0693-2026
ClassificationClass II
FDA statusOngoing
Origin on fileSanta Fe Springs CA United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.