Medline Renewal recalls ENT Coblator II PROcise XP Wand with integrated suction and saline. Drip chambers may disconnect from saline tubing when under tension, potentially causing saline flow issues during use.
Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
Medline Renewal is recalling ENT Coblator II PROcise XP Wands with integrated suction and saline systems. The recall is due to a risk that drip chambers may disconnect from the saline line tubing when under tension, which could lead to saline flow problems during procedures.
The drip chambers in affected devices may disconnect from the saline line tubing when under tension. This could cause saline flow interruptions during procedures, potentially leading to inadequate irrigation or saline delivery.
Owners of Medline Renewal ENT Coblator II PROcise XP Wands with integrated suction and saline systems are affected. Dental and ENT professionals using these devices are most at risk due to potential saline flow issues during procedures.
Check for the blue color and item number REF EICA88720R on the device. Affected units have specific lot numbers listed in the recall notice.
Look for lot numbers 506894, 509420, 512983, and other listed numbers on the device.
The drip chambers may disconnect from the saline line tubing when under tension, which could cause saline flow interruptions during procedures.
Check for the blue color and item number REF EICA88720R. Affected units have specific lot numbers listed in the recall notice.
The recall record does not specify a remedy.
We’ve drafted a message you can send Medline Renewal to request your refund or repair — edit it as you like.
Subject: Recall Z-1548-2025 — Medline Renewal Medline Renewal Hello, I own a Medline Renewal that is covered by recall Z-1548-2025 from Medline Renewal. 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.
