Class II

Medical Device Recall: Stimuplex A, 30 DEG, 22GX2", 0.70x50mm, Catalogue Number: 4894502

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

1,157,640 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2134-2024

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.