Medline recalls ReNewal Coblator II Evac 70 Xtra Plasma Wands with potential drip chamber disconnection under tension. Affected units have specific lot numbers and item numbers. Stop using immediately to prevent saline line disconnection.
Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
Medline is recalling ReNewal Coblator II Evac 70 Xtra Plasma Wands that may disconnect the drip chamber from the saline line when under tension. This could lead to improper saline flow during medical procedures, potentially causing complications for users.
The drip chambers in affected devices may disconnect from the saline line tubing when the device is pulled or stressed. This could cause improper saline flow during medical procedures, potentially leading to complications for patients.
Medical professionals using the ReNewal Coblator II Evac 70 Xtra Plasma Wand for procedures are most at risk. Patients receiving treatments with this device could face complications if the saline line disconnects.
Check for the item number REF EICA58720R on the device. Affected units have specific lot numbers listed in the recall notice, including 513468 through 529932.
Discontinue use of the affected ReNewal Coblator II Evac 70 Xtra Plasma Wand to prevent potential saline line disconnection.
The recalled device is the Medline ReNewal Coblator II Evac 70 Xtra Plasma Wand with integrated saline line and cable, item number REF EICA58720R.
Check for the item number REF EICA58720R and the specific lot numbers listed in the recall notice, which include 513468 through 529932.
Stop using the device immediately and contact Medline for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1546-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1546-2025 from Medline. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
