CLASS II Device recall · Reported 23 Oct 2019 · FDA Enforcement Report
Cautery Tip Cleaner recalled by Xodus Medical
Xodus Medical is recalling Cautery Tip Cleaner, distributed nationwide in the US. The recall was initiated on 19 Sep 2019 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-0151-2020
- FDA event ID
- 83819
- Recalling firm
- Xodus Medical, New Kensington, PA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 19 Sep 2019
- FDA classified
- 16 Oct 2019
- Reported
- 23 Oct 2019
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Sterility
- Device type
- Surgical Instruments
Timeline
| 19 Sep 2019 | Recall initiated by company | |
| 16 Oct 2019 | Classified by FDA | +27 days |
| 23 Oct 2019 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The sterile barrier of some devices may have been affected
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
Cautery Tip Cleaner REF: 30500 Product Usage: electrosurgical accessory
Where it was distributed
Worldwide Distribution - US Nationwide in the States of : CA, ID, IL, LA, MD, NY, OH, OK, TX, VA, WI and OUS: Malaysia, Kuwait, Australia, Canada, UAE, Ireland, Korea, Saudi Arabia, Japan, Mexico
Nationwide CaliforniaIdahoIllinoisLouisianaMarylandNew YorkOhioOklahomaTexasVirginiaWisconsin
Questions about this recall
Is Cautery Tip Cleaner recalled?
Yes. Xodus Medical recalled Cautery Tip Cleaner on 19 Sep 2019. The recall is Class II and its status is Terminated. Recall number Z-0151-2020.
Why was it recalled?
The sterile barrier of some devices may have been affected
Which lots are affected?
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
Where was it sold?
Worldwide Distribution - US Nationwide in the States of : CA, ID, IL, LA, MD, NY, OH, OK, TX, VA, WI and OUS: Malaysia, Kuwait, Australia, Canada, UAE, Ireland, Korea, Saudi Arabia, Japan, Mexico
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Xodus Medical
All 3| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Electrosurgical Tip Cleaner recalled by Xodus Medical | Xodus Medical | Sterility | Nationwide |
| Device | CLASS II | Electrosurgical Tip Cleaner recalled by Xodus Medical | Xodus Medical | Sterility | Nationwide |
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All 3,809| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Medline Convenience Kits: IV Start KIT recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing BD ChloraPrep Clear recalled | Medline Industries | Lead & Heavy Metals | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: Open Heart Pack, Medline Kit recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: GYN Robotic CDS, Medline Kit recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Linvatec Genesys CrossFT Suture Anchor with Disposable Driver recalled | ConMed | Sterility | Nationwide |