MEDLINE INDUSTRIES, LP - Northfield: Medical Device Recall in 2025 - (Recall #: Z-1547-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

MEDLINE ReNewal Coblator II ENT Evac 70 Xtra HP,w/Integrated Cable (Blue/Grey), Number REF EICA58740R

Product Classification:

Class II

Date Initiated: March 5, 2025

Date Posted: April 16, 2025

Recall Number: Z-1547-2025

Event ID: 96541

Reason for Recall:

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

Status: Ongoing

Product Quantity: 020 units

Code Information:

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.

Distribution Pattern:

US Nationwide distribution

Voluntary or Mandated:

Voluntary: Firm initiated