Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MEDLINE ReNewal ENT Coblator II PROcise mAx Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline ReNewal has identified that the drip chambers...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact MEDLINE INDUSTRIES, LP - Northfield directly.
Affected Products
MEDLINE ReNewal ENT Coblator II PROcise mAx,W/ Integrated Cable Suction & Saline (Blue), Item Number REF EICA88980R
Quantity: 224 units
Why Was This Recalled?
Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About MEDLINE INDUSTRIES, LP - Northfield
MEDLINE INDUSTRIES, LP - Northfield has 822 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report