Class II
Medical Device Recall: ANESTHESIA TURNOVER KIT, Pack Number DYNJAA0377
MEDLINE INDUSTRIES, LP - Northfield · June 18, 2024
Reason for Recall
A non-sterile Mastisol component, which was not labeled as being sterile or non-sterile, was placed in the non-sterile portion of certain sterile convenience kits and distributed. In the event that the user assumes sterility during its use, there is an increased risk of patient infection.
Distribution
US: TX, IL, CA
States Affected
CA, IL, TX
Quantity Affected
105 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-3071-2024
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.