D-0693-2026 Class II Ongoing

Recalled by Blaine Labs Inc — Santa Fe Springs, CA

FDA drug recall D-0693-2026 was initiated by Blaine Labs Inc on April 8, 2026 and is designated Class II. Reason for recall: CGMP Deviations: product manufactured in the same facility under the same conditions as the product found to be contaminated The recall status is ongoing. Affected quantity: 519 - 1 oz bottles.

Recall Details

Product Type
Drugs
Report Date
July 8, 2026
Initiation Date
April 8, 2026
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
519 - 1 oz bottles

Product Description

TRIFLUENT 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.

Reason for Recall

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

Distribution Pattern

Nationwide in the USA

Code Information

Lot #: BL3435, Exp. 11/06/26