Medline Renewal ENT Coblator II PROcise XP Wand Recall: Drip Chamber Disconnects Under
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.
Lower-risk recall
Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/52668-medline-renewal-ent-coblator-ii-procise-xp-wand-recall-drip.
Source Summary by GovInfoNow · govinfonow.com/recall/52668-medline-renewal-ent-coblator-ii-procise-xp-wand-recall-drip · Updated August 18, 2026 · FDA enforcement record: FDA #Z-1548-2025
Cite this page
“Medline Renewal ENT Coblator II PROcise XP Wand Recall: Drip Chamber Disconnects Under.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/52668-medline-renewal-ent-coblator-ii-procise-xp-wand-recall-drip. Based on FDA recall #Z-1548-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1548-2025%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
Check for the blue color and item number REF EICA88720R on the device. Affected units have specific lot numbers listed in the recall notice.
- Brand
Medline Renewal- Category
Medical device
All 4 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Ongoing- Distribution
US Nationwide distribution
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-1546-2025 | MEDLINE ReNewal Coblator II Evac 70 Xtra Plasma Wand,w/Integrated Saline Line & Integrated Cable, Item Number REF EICA58720R; UDI/DI 10888277395350, Lot Numbers: 513468, 513993, 514445, 514446, 514449, 515558, 515650, 515861, 515907, 516476, 516478, 516549, 517320, 517321, 517322, 517323, 517358, 517360, 517627, 517628, 517631, 518473, 518476, 518477, 518960, 519256, 519257, 519258, 519260, 519264, 519265, 519678, 519759, 519760, 519762, 519860, 519965, 519967, 520279, 520357, 520358, 520691, 520692, 521358, 521359, 522140, 522141, 522142, 522143, 522506, 522507, 522508, 522510, 524010, 524011, 524015, 524798, 524801, 524802, 524822, 525470, 525474, 527114, 527117, 528453, 528455, 528583, 528585, 528586, 528896, 528899, 528902, 528903, 528904, 529481, 529491, 529931, 529932, 530010, 530435, 531018, 531025, 531026, 531027, 531672, 532270, 532272, 532815, 532817, 532819, 532822. | 738 units |
| Z-1547-2025 | MEDLINE ReNewal Coblator II ENT Evac 70 Xtra HP,w/Integrated Cable (Blue/Grey), Number REF EICA58740R; UDI/DI 10888277395367, Lot Numbers: 513993, 514445, 514446, 514449, 515558, 515650, 515861, 515902, 515907, 516478, 516549, 517320, 518476, 519258, 519265, 519678, 519759, 519760, 520279, 520282, 520357, 520692, 521356, 521359, 522140, 522141, 522143, 522507, 522508, 524010, 524011, 524015, 524797, 524798, 524802, 528455, 528586, 528587, 528896, 528904, 529932, 530010, 531025, 531027, 532815, 532817. | 020 units |
| Z-1548-2025 | MEDLINE ReNewal ENT Coblator II PROcise XP Wand,w/Integrated Cable Suction & Saline (Blue), Item Number REF EICA88720R; UDI/DI 10888277395374, Lot Numbers: 506894, 509420, 512983, 513469, 514448, 514549, 515557, 515860, 515903, 516550, 517359, 517626, 519259, 519413, 519966, 520277, 521360, 522144, 522145, 525472, 527111, 527115, 527121, 528456, 528457, 528582, 529483, 529485, 529487, 529489, 529930, 530432, 530433, 530434, 531020, 531024, 531676. | 315 units |
| Z-1549-2025 | MEDLINE ReNewal ENT Coblator II PROcise mAx,W/ Integrated Cable Suction & Saline (Blue), Item Number REF EICA88980R; UDI/DI 10080196415106, Lot Numbers: 506549, 508766, 509420, 512036, 512983, 514060, 514709, 516475, 516802, 517626, 518478, 518961, 519248, 519259, 519411, 519412, 519413, 519966, 519969, 520277, 522144, 522145, 527110, 527112, 528454, 528458, 528584, 531021, 531022. | 224 units |
What to do — step by step
Check Device Lot Number
Look for lot numbers 506894, 509420, 512983, and other listed numbers on the device.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide distribution” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 42 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-1548-2025 (March 5, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1548-2025 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.