Class I

Medical Device Recall: MEDLINE ARTERIAL BUNDLE NO CATHETER, REF ART995

MEDLINE INDUSTRIES, LP - Northfield · November 15, 2023

Reason for Recall

Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.

Distribution

Distribution US nationwide including Puerto Rico, Canada, UAE, and Panama

States Affected

NATIONWIDE

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1094-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.