PlainRecalls
FDA Devices Moderate Class II Terminated

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

Reported: May 23, 2018 Initiated: March 11, 2018 #Z-1868-2018

Product Description

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

Reason for Recall

Tube ends may be mixed up.

Details

Recalling Firm
Richard Wolf GmbH
Units Affected
1710 units
Distribution
Worldwide Distribution
Location
Knittlingen

Frequently Asked Questions

What product was recalled?
RICHARD WOLF TUBE SET FOR TEM, REF 4170.801. Used for the transanal endoscopic microsurgery.. Recalled by Richard Wolf GmbH. Units affected: 1710 units.
Why was this product recalled?
Tube ends may be mixed up.
Which agency issued this recall?
This recall was issued by the FDA Devices on May 23, 2018. Severity: Moderate. Recall number: Z-1868-2018.