MEDLINE INDUSTRIES, LP - Northfield: Medical Device Recall in 2025 - (Recall #: Z-1548-2025)

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 ENT Coblator II PROcise XP Wand,w/Integrated Cable Suction & Saline (Blue), Item Number REF EICA88720R

Product Classification:

Class II

Date Initiated: March 5, 2025

Date Posted: April 16, 2025

Recall Number: Z-1548-2025

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: 315 units

Code Information:

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.

Distribution Pattern:

US Nationwide distribution

Voluntary or Mandated:

Voluntary: Firm initiated