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Terminated

Microtek Medical, Inc. ORS Fluid Warming and Slush Drapes, Model #'s ORS-100, ORS-110, ORS-130, ORS-300, ORS-301, ORS-320, ORS-321, ORS-325, ORS-330, ORS-331 and ORS-2200. The ORS Fluid Warming and Slush Drapes are individually wrapped and placed in poly-Tyvek pouches with a label insert, then packaged as 24 per case in a labeled corrugated shipper box. Intended for use during various surgeries where warm irrigation, slush and/or cold solution are required.

FDA Recall Z-2793-2015 · Posted 2015-09-18

Recalling FirmEcolab Inc
Recall StatusTerminated
Product CodeLHC
Date Initiated2015-08-18
Date Terminated2017-08-09
Product Quantity5,172,816 units

Reason for Recall

The sterile packaging may contain small (less than 250 microns wide) channels in the seal of the pouch. If channels are present, the package integrity is compromised and there is a remote chance that a non-sterile drape may be used during a surgical procedure.

Firm Action

Consignees were sent on 8/18/2015 an Ecolab "Urgent Medical Device Recall" letter dated August 18, 2015. The letter was addressed to Recall Coordinator or Risk Manager. The letter described the problem and the product involved in the recall. Advised consignees to quarantine all affected lots, and notify their customers of the recall which is to be carried out to users level. Requested consignees to complete and return the enclosed Recall Response Form. For questions they can contact Customer Service at 1-800-824-3027 or e-mail [email protected].

Root Cause

Package design/selection

Distribution Pattern

Worldwide Distribution -- US, including DC and PR; and, the countries of SAUDI ARABIA, LEBANON, GERMANY, HONG KONG, SINGAPORE, CANADA, and JAPAN.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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