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RecallWatchMedical Device Safety
Class IIOngoingZ-1548-2025

MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE ReNewal ENT Coblator II PROcise XP Wand

MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesReported Apr 16, 2025 · 1 year ago
Legal News Analyst ·

Reason for recall

Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.

Affected product

Check your device

Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.

Affected products & lots

  • MEDLINE ReNewal ENT Coblator II PROcise XP Wand,w/Integrated Cable Suction & Saline (Blue), Item Number REFEICA88720R
    37 affected lots
    506894509420512983513469514448514549515557515860
    +29 more515903516550517359517626519259519413519966520277521360522144522145525472527111527115527121528456528457528582529483529485529487529489529930530432530433530434531020531024531676

What the firm is doing

Medline issued a "Medline ReNewal IMMEDIATE ACTION REQUIRED" notice dated 3/5/2025, to its consignees on 03/05/2025 via USPS first class mail. The notice explained the issue, potential risk, and requested the following actions: REQUIRED ACTION: 1. Immediately check your stock for the affected item numbers and the affected lot numbers. Quarantine all affected product. 2. Please return the completed enclosed response form listing the quantity of affected product on hand. Upon receipt of your submitted response form, FedEx return label(s) will be provided. Even if you do not have any affected product, please complete and return the form, as indicated on the response form. 3. If you have transferred possession of this product to another individual, to another department or another location in your organization you are required to notify them of this recall communication. Have the customers return any affected product to you for collection and return to Medline ReNewal. For questions, please contact 866-359-1704 or recalls@medline.com.

DistributionShow details

US Nationwide distribution

Class IIWhat this means

Use of the product may cause temporary or medically reversible adverse health consequences.

Sources & references

Taylor Coteus
Legal News Analyst

Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.

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