ClearanceBrief
Recall Z-2193-2023 ยท CBT Arterial Blood Sampling Kit

MEDLINE INDUSTRIES, LP - Northfield

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

DateJul 20, 2023 (initiated May 18, 2023)
StatusOpen, Classified
ReasonProbe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
Root causeDevice Design
ActionMedline distributed their recall notices to their consignees beginning on 05/18/2023 by letter. The notices explained the problem, and the risk and requested the destruction of the products. Distributors were directed to notify their consignees, have the customers document and destroy any affected product, and include your customers quantities on the response form. Beginning on 05/23/2023, Medline issued another notice to a separate group of consignees requesting that the kits be over labeled. Distributors were directed to notify the customers and have them return any affected product to
Quantity2590 units
DistributionWorldwide Distribution: US (Nationwide) and OUS (foreign) United Arab Emirates, Singapore, Lebanon, China Qatar, Costa Rica, India, Canada, Panama & Saudi Arabia.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.