Covidien LLC: Medical Device Recall in 2014 - (Recall #: Z-1997-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Devon Supine, Lithotomy and Trendelenburg Positioning Kit; Product Code: 31151090 Product Usage: The device is intended to provide padding under the patient, and help maintain the position of an anesthetized patient during surgery.

Product Classification:

Class II

Date Initiated: May 8, 2014

Date Posted: July 16, 2014

Recall Number: Z-1997-2014

Event ID: 68243

Reason for Recall:

Straps may separate from the foam pad.

Status: Terminated

Product Quantity: 264 devices

Code Information:

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.

Distribution Pattern:

US Nationwide Distribution in the states of NJ, CA, TX, IL, MO, PA, OH, IN, MI, MN, FL, IN, DC, PA, VA, MS, ME, NV, AR, KY, NY, KS, SC

Voluntary or Mandated:

Voluntary: Firm initiated