Class II
Medical Device Recall: Baxter Seprafilm Adhesion Barrier 1 Half Sheet, 5-PK, REF 664103, for use in abdominal and pelvic surgery
Baxter Healthcare Corporation · March 15, 2024
Reason for Recall
Product was distributed in the United States without proper regulatory approval.
Distribution
US Nationwide distribution in the states of LA, GA, IN, VA FL, NY, CA.
States Affected
NATIONWIDE
Quantity Affected
165 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1689-2024
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.