Biocompatibles UK recalls Varithena injectable foam packs with defective syringes. Incorrect syringes may cause improper medication delivery. Consumers should check product details and contact the company for remedies.
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).
Biocompatibles UK recalls Varithena injectable foam packs that contain the wrong type of syringes. Using these packs could lead to incorrect medication delivery, which might affect treatment effectiveness.
The recall involves packs that include incorrect syringes (NormJect 10 mL Luer Lock Solo) instead of the required silicone oil-free NormJect 10 mL Luer Solo syringes. This mismatch could lead to improper medication delivery during injections.
People who have received Varithena injectable foam packs with the specific lot numbers listed in the recall. Those using the product for medical treatments are most at risk.
Check the product label for lot numbers 34067418 or 34067419, which expire in March 2026. The product includes 3 silicone-free syringes, 2 compression pads, and 1 Varithena Transfer Unit.
Look for lot numbers 34067418 or 34067419 on the packaging, which expire in March 2026.
The recall involves packs that contain incorrect syringes (NormJect 10 mL Luer Lock Solo) instead of the required silicone oil-free NormJect 10 mL Luer Solo syringes.
Check the product label for lot numbers 34067418 or 34067419, which expire in March 2026.
The recall does not specify a remedy, so contact Biocompatibles UK directly for further instructions.
We’ve drafted a message you can send Biocompatibles to request your refund or repair — edit it as you like.
Subject: Recall D-0113-2025 — Biocompatibles Biocompatibles Hello, I own a Biocompatibles that is covered by recall D-0113-2025 from Biocompatibles. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
