Covidien LLC: Medical Device Recall in 2017 - (Recall #: Z-1409-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Premier Guard Drape, Sterile. For Use with Verisphere (01-0035) and ArQ.Sphere (01-0044) Item Number: 01-0037 Used in conjunction RF Surgical Gauze detection systems to protect scanning device from contamination during various surgical procedures

Product Classification:

Class II

Date Initiated: January 23, 2017

Date Posted: March 15, 2017

Recall Number: Z-1409-2017

Event ID: 76327

Reason for Recall:

Sterility compromised due to breach in sterile barrier

Status: Terminated

Product Quantity: 42,750 units

Code Information:

Lot Numbers: 1410577-4 to 1605778

Distribution Pattern:

Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated