Ecolab recalls ORS-320 Slush + Warmer Disc Drapes with slits that could breach sterile barriers, risking infection during surgery. Affected units: 132 cases (3168 drapes) from lot D192619A.
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.
Ecolab is recalling ORS-320 Slush + Warmer Disc Drapes that have slits in a small number of units. These slits could break the sterile barrier between fluid and equipment, potentially causing infections during surgery if used.
The slits in the drapes may allow fluid to leak through the sterile barrier. This could expose patients to infection during surgery when warm irrigation or slush is used.
Healthcare workers using the ORS-320 Slush + Warmer Disc Drapes for surgical procedures are most at risk. Patients receiving warmed irrigation fluid or surgical slush could be affected if the recalled drapes are used.
Check for the model number ORS-320 on the drape packaging. The affected lot is D192619A, sold in 132 cases (3168 drapes) for surgical use.
Look for the model number ORS-320 and lot number D192619A on the drape packaging.
The recall is for a small number of drapes with slits that could breach the sterile barrier. Most units are safe, but affected units should be checked.
132 cases (3,168 drapes) from lot D192619A.
Check the packaging for model ORS-320 and lot D192619A. If you have these, contact Ecolab for guidance.
We’ve drafted a message you can send Ecolab to request your refund or repair — edit it as you like.
Subject: Recall Z-1141-2021 — Ecolab Ecolab Hello, I own a Ecolab that is covered by recall Z-1141-2021 from Ecolab. 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.
