WhichRecall
Class IIIReported 2024-12-18

Varithena (polidocanol injectable foam) Administration Pack, Contains: 3 silicone-free syringes, 2 compression pads, 1 Varithena Transfer Unit, 1 manometer tubing, Rx Only, Distributed by Biocompatibles Inc., a BTG International Group company. CN01114.3

Recalled by Biocompatibles UK, Ltd.

Reason for Recall

Defective Delivery System: incorrect silicone oil-free NormJect 10 mL Luer Lock Solo syringes packaged in the pack, instead of the required silicone oil-free NormJect 10 mL Luer Solo syringes (luer slip connection).

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Recall Number
D-0113-2025
Classification
Class III
Status
Terminated
Category
drug
Initiated
2024-08-15
Reported
2024-12-18
Distribution
Nationwide in the USA.
Code Info
Lot # 34067418, Exp. March 2026, 34067419, Exp. March 2026
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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