Data Foundry

Medical device recalls 2019

Cautery Tip Cleaner REF: 30500 Product Usage: electrosurgical… — Class II medical device recall Z-0151-2020

Terminated recall by Xodus Medical Inc, reported 2019-10-23, distributed nationwide. The sterile barrier of some devices may have been affected

Recall numberZ-0151-2020
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmXodus Medical Inc, New Kensington, PA, United States
Recall initiated2019-09-19
Classified2019-10-16
Reported by FDA2019-10-23
Terminated2024-03-04
DistributedNationwide (US)
Countries outside the USAE, AU, CA, IE, JP, KR, KW, MX, MY, SA
Quantity255,000 units
Reason classessterility
UPC / GTIN / UDI-DI00787551000573, 20787551000577
Lot numbers16DEC19, 17APR03, 17APR14, 17AUG01, 17DEC15, 17FEB27, 17JAN06, 17JAN06A, 17JAN23, 17JUL17, 17JUN27, 17MAR13, 17MAR13A, 17MAY24, 17MAY24A, 17MAY24B, 17NOV27, 17NOV27A, 17OCT23, 17SEP22, 17SEP22A, 18FEB16, 18JAN19, 18JAN19A, 18MAR02, 18MAR19, 18MAR19A, 19MAR14
Model numbers30500

Product

Cautery Tip Cleaner REF: 30500 Product Usage: electrosurgical accessory

Reason for recall

The sterile barrier of some devices may have been affected

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0151-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.