RecallRadar

FDA Device recall Z-0151-2020

Cautery Tip Cleaner REF: 30500 Product Usage: electrosurgical accessory

On 2019-10-23 the FDA classified a Class II recall of Cautery Tip Cleaner REF: 30500 Product Usage: electrosurgical accessory by Xodus Medical, citing the sterile barrier of some devices may have been affected.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0151-2020
ClassificationClass II
Statusterminated
Initiated2019-09-19
Published2019-10-23
Last updated2026-09-13 11:55 UTC
CompanyXodus Medical
DistributionUS

Product

Cautery Tip Cleaner REF: 30500 Product Usage: electrosurgical accessory

Reason

The sterile barrier of some devices may have been affected

Identifiers

code_info
Lot # 16DEC19 17JAN06 17JAN06A 17JAN23 17FEB27 17MAR13 17MAR13A 17APR03 17APR14 17MAY24 17MAY24A 17MAY24B 17JUN27 17JUL…Lot # 16DEC19 17JAN06 17JAN06A 17JAN23 17FEB27 17MAR13 17MAR13A 17APR03 17APR14 17MAY24 17MAY24A 17MAY24B 17JUN27 17JUL17 17AUG01 17SEP22 17SEP22A 17OCT23 17NOV27 17NOV27A 17DEC15 18JAN19 18JAN19A 18FEB16 18MAR02 18MAR19 18MAR19A ***Updated 11/9/21*** 19MAR14 UDI: Case 20787551000577 and Each 00787551000573

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0151-2020%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.