Richard Wolf GmbH: Medical Device Recall in 2018 - (Recall #: Z-2897-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Artholine Punch B 4, 6MM H 1, 6MM, used for the removal of soft tissue, cartilage tissue or other non-osseous tissue via natural or surgically created passages. Product Usage: Device is a standard punch; standard punches are used for the removal of soft tissue, cartilage tissue or other non-osseous tissue via natural or surgically created passages.

Product Classification:

Class II

Date Initiated: July 24, 2017

Date Posted: August 29, 2018

Recall Number: Z-2897-2018

Event ID: 80583

Reason for Recall:

Punch may have a burr in one section of the joint and when the punch is open, there is an increase potential for injury.

Status: Ongoing

Product Quantity: 12 units

Code Information:

Product Number 89140.0105, Lot Number 4500197481

Distribution Pattern:

Worldwide distribution to Germany, Hong Kong, Ireland, Romania, and Turkey.

Voluntary or Mandated:

Voluntary: Firm initiated