Reported Jul 16, 2014 · Terminated

Devon Supine, Lithotomy and Trendelenburg Positioning Kit; Product Code: 31151090 Product Usage: The device is intended…

Covidien LLC

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: Covidien LLC · 15 Hampshire Street · Mansfield, MA · 02048-1113

Is this the product you have?

  • Devon Supine, Lithotomy and Trendelenburg Positioning Kit
  • Product Code31151090
  • Product UsageThe device is intended to provide padding under the patient, and help maintain the position of an anesthetized patient during surgery
Lot codes and dates
  • 14085, 14086, 14092, 14095, 14101, 14106 *The original recall submission listed 14084 and 14094, these were reported by Covidien in error on the original submission.
Amount recalled
264 devices

Where it was sold

Why it was recalled

Straps may separate from the foam pad.

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 Sep 4, 2015 · Data as of Sep 19, 6:00 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.