Richard Wolf GmbH: Medical Device Recall in 2018 - (Recall #: Z-1868-2018)

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:

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

Product Classification:

Class II

Date Initiated: March 11, 2018

Date Posted: May 23, 2018

Recall Number: Z-1868-2018

Event ID: 79886

Reason for Recall:

Tube ends may be mixed up.

Status: Terminated

Product Quantity: 1710 units

Code Information:

Lot numbers: 32062417, 32133317

Distribution Pattern:

Worldwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated