FDAJanuary 11, 2021device

Slush + Warmer Disc Drape; Model ORS-320 Slush + Warmer Disc Drapes - Product Usage: single-use equipment cover intended for use during various surgeries where warm irrigation, slush and/or cold solution is required.

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

The hazard

Slits were identified in a low quantity of ORS-320 Slush + Warmer Disc Drapes from a single lot. A source for potential manufacturing error was identified and investigation is underway to prevent further recurrence. The slits may lead to a breach in the sterile barrier between fluid in the basin and the slush/warming equipment. This could pose a risk of infection to patients receiving warmed irrigation fluid or surgical slush if used during a procedure.

What to do

FDA enforcement status: Terminated

Brands named

ecolab

Recall history

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

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