MEDLINE ReNewal ENT Coblator II PROcise XP Wand,w/Integrated Cable Suction & Saline (Blue), Item Number REF EICA88720R
Reported: April 16, 2025 Initiated: March 5, 2025 #Z-1548-2025
Product Description
MEDLINE ReNewal ENT Coblator II PROcise XP Wand,w/Integrated Cable Suction & Saline (Blue), Item Number REF EICA88720R
Reason for Recall
Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
Details
- Recalling Firm
- MEDLINE INDUSTRIES, LP - Northfield
- Units Affected
- 315 units
- Distribution
- US Nationwide distribution
- Location
- Northfield, IL
Frequently Asked Questions
What product was recalled? ▼
MEDLINE ReNewal ENT Coblator II PROcise XP Wand,w/Integrated Cable Suction & Saline (Blue), Item Number REF EICA88720R. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 315 units.
Why was this product recalled? ▼
Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 16, 2025. Severity: Moderate. Recall number: Z-1548-2025.
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