Molnlycke Health Care, Inc: Medical Device Recall in 2017 - (Recall #: Z-2110-2017)

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:

Brennen Skin Graft Mesher. Surgical instrument designed to expand skin grafts'

Product Classification:

Class II

Date Initiated: April 24, 2017

Date Posted: May 24, 2017

Recall Number: Z-2110-2017

Event ID: 77121

Reason for Recall:

Sterilization validation failure.

Status: Ongoing

Product Quantity: 956 units

Code Information:

Code: 131600, 131601, 131602, 131603, 131604, 131500, 131501, 131502, 131503, 131504 and 131506.

Distribution Pattern:

Domestic: U.S. Nationwide; Foreign: Austria, Australia, Bangladesh, Canada, Chile, Germany, Denmark, Finland, France, Great Britain, Hong Kong, Hungary, Ireland, India, Italy, Jordan, Korea, Kuwait, Malaysia, Norway, New Zealand, Peru, Saudi Arabia, Sweden Switzerland, Taiwan, Turkey, South Africa, United Arab Emirates.

Voluntary or Mandated:

Voluntary: Firm initiated