Covidien LLC: Medical Device Recall in 2015 - (Recall #: Z-2109-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Minor Surgical Kits, Sterile-Kits containing the Devon Light Glove Catalog Numbers/Description: 573208 7519-DHCG MINOR KIT 573210 7581-CSD Minor KIT 573741 7667-HMI Minor Kit 31144507 7519 Minor Surgical Kit 573830D MINOR KIT

Product Classification:

Class II

Date Initiated: April 16, 2015

Date Posted: July 29, 2015

Recall Number: Z-2109-2015

Event ID: 71113

Reason for Recall:

Devon Light Gloves contain splits or holes compromising the sterility

Status: Terminated

Product Quantity: 81,252 kits

Code Information:

Lot number begins 508xxxx or lower

Distribution Pattern:

Worldwide Distribution-US (nationwide) including the Virgin Islands and the countries of Canada, Australia, New Zealand, Costa Rica, Austria, Belgium, Bulgaria, Czech Republic, Denmark, Finland , France, Germany, Netherlands, Sweden, Ireland, ISRAEL,Spain, Italy, Jordan, Kenya, Kuwait, United Kingdom, Lebanon, Liechtenstein, Luxembourg, Monaco, South Africa, Norway, Poland, Portugal, Qatar, Russia, Saudi Arabia, Slovenia, Switzerland, Turkey, and UAE.

Voluntary or Mandated:

Voluntary: Firm initiated