MEDLINE INDUSTRIES, LP - Northfield: Medical Device Recall in 2023 - (Recall #: Z-2193-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) RADIAL ARTERIAL LINE KIT, Model Number ART1070A; b) ARTERIAL LINE START KIT, Model Number ART1160; c) ARTERIAL LINE TRAY W/O CATHETER, Model Number ART1180; d) ARTERIAL LINE INSERTION KIT, Model Number ART775B; e) ARTERIAL LINE KIT W/O CATHETER, Model Number ART890A; f) ARTERIAL BUNDLE NO CATHETER, Model Number ART995; g) ARTERIAL LINE START KIT W/O CATH, Model Number P42453;

Product Classification:

Class II

Date Initiated: May 18, 2023

Date Posted: July 26, 2023

Recall Number: Z-2193-2023

Event ID: 92466

Reason for Recall:

Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.

Status: Ongoing

Product Quantity: 2590 units

Code Information:

all lots within expiry, distributed from Medline between December 2017 May 2023: a) Model Number ART1070A, UDI/DI EA 10653160358329, UDI/DI CS 00653160358322; b) Model Number ART1160, UDI/DI EA 10653160355762, UDI/DI CS 00653160355765; c) Model Number ART1180, UDI/DI EA 10653160355472, UDI/DI CS 00653160355475; d) Model Number ART775B, UDI/DI EA 10653160353560, UDI/DI CS 00653160353563; e) Model Number ART890A, UDI/DI EA 10653160356677, UDI/DI CS 00653160356670; f) Model Number ART995, UDI/DI EA 10193489190502, UDI/DI CS 20193489190509; g) Model Number P42453, UDI/DI EA 10653160323792, UDI/DI CS 00653160323795

Distribution Pattern:

Worldwide Distribution: US (Nationwide) and OUS (foreign) United Arab Emirates, Singapore, Lebanon, China Qatar, Costa Rica, India, Canada, Panama & Saudi Arabia.

Voluntary or Mandated:

Voluntary: Firm initiated