Richard Wolf GmbH: Medical Device Recalls in 2018

According to to data from the FDA, there were 2 medical device recalls made by Richard Wolf GmbH in 2018. See the details of the recalls below.

You can see similar recalls for other firms.

• RICHARD WOLF TUBE SET FOR TEM, REF 4170.801. Used for the transanal endoscopic microsurgery.
• 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.