MEDLINE INDUSTRIES, LP - Northfield: Medical Device Recall in 2025 - (Recall #: Z-1549-2025)

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 mAx,W/ Integrated Cable Suction & Saline (Blue), Item Number REF EICA88980R

Product Classification:

Class II

Date Initiated: March 5, 2025

Date Posted: April 16, 2025

Recall Number: Z-1549-2025

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: 224 units

Code Information:

UDI/DI 10080196415106, Lot Numbers: 506549, 508766, 509420, 512036, 512983, 514060, 514709, 516475, 516802, 517626, 518478, 518961, 519248, 519259, 519411, 519412, 519413, 519966, 519969, 520277, 522144, 522145, 527110, 527112, 528454, 528458, 528584, 531021, 531022.

Distribution Pattern:

US Nationwide distribution

Voluntary or Mandated:

Voluntary: Firm initiated