Class II
Medical Device Recall: Stimuplex A, 30 DEG, 20GX6", 0.90x150mm, Catalogue Number: 4894278
B Braun Medical Inc · May 17, 2024
Reason for Recall
The devices are labeled "not made with DEHP" or the DEHP free symbol; however, the glue used contains traces of DEHP.
Distribution
Worldwide distribution - US Nationwide and the country of Canada.
States Affected
NATIONWIDE
Quantity Affected
108,811 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2133-2024
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.