FDASeptember 28, 2017device

V-PRO 60 Low Temperature Sterilization System (UDI: 00724995152000)

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

The hazard

Correction to update sterilizer software to prohibit the use of expired sterilant prior to the start of a sterilization cycle.

What to do

FDA enforcement status: Terminated

Brands named

steris

UPCs

00724995152000

Recall history

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

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V-PRO 60 Low Temperature Sterilization System (UDI: 00724995152000) — Recall Details · AllClear