Reported Oct 31, 2018 · Terminated

Disposable Accessory Kit, 3-Arm (Box of 5) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively…

Ecolab Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Ecolab Inc · 1 Ecolab Pl · Saint Paul, MN · 55102-2739

Is this the product you have?

  • Disposable Accessory Kit, 3-Arm (Box of 5) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively on the Intuitive Surgical Da Vinci Si Robotic system / Distributed
  • by Intuitive Surgical Product UsageMicrotek Medical Equipment Drapes are intended to cover/wrap various surgical and/or nonsurgical instruments/equipment [e.g. robotic arms, microscopes, tables, x ray systems, light handles, etc]. They function as a physical barrier to prevent cross contamination between the instrument / equipment and medical staff and/or to allow the instrument/equipment to enter a hygienic area [e.g. sterile surgical field] in various clinical settings. They are typically made of flexible plastic and shaped to fit the type of instrument / equipment. They are a single use device [not to be reprocessed]
Lot codes and dates
    • Item 420290-03 Lots # D173047
    • D173557
    • D173017
    • D180127
    • D172917
    • D180137
    • D172827
    • D172897
    • D180197A
    • D172757
    • D173037
    • D173557A
    • D180297
    • D172907
    • D180127A
    • D173207
    • D172847
    • D180397
    • D180037
    • D180287
    • D180267
    • D180197
    • D180277
    • D180417
    • D172787
    • D180047
    • D173057
    • D180407
    • D172797
    • D173567
    • D180477
    • and D180607
Amount recalled
4,861 cases (24,305 eaches)

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

Why it was recalled

The pouches of certain lots of product may have wrinkles along the pouch seal that could result in a channel within the seal. Should there be a channel in the pouch seal it may result in a breach in the sterility of the product.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Feb 12, 2021 · Data as of Sep 19, 5:33 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.