Class II
Medical Device Recall: RUMMELL, Medline Item No. ST006ST
MEDLINE INDUSTRIES, LP - Northfield · November 12, 2024
Reason for Recall
Weak seals may result in a breach of sterility, which may not be detectable to the user. This can lead to increased risk of contamination and infection.
Distribution
US Nationwide distribution.
States Affected
NATIONWIDE
Quantity Affected
21,440 total
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0760-2025
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.