FDADecember 16, 2025device

Vortex Surgical 25GA Backflush, VS0270.25; 25GA Backflush Retractable, VS0275.27

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.

What to do

FDA enforcement status: Ongoing

Brands named

vortex surgicalvortex

UPCs

810123480470810123480753810123480517810123480791

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Vortex Surgical 25GA Backflush, VS0270.25; 25GA Backflush Retractable, VS0275.27 — Recall Details · AllClear