Class II
Medical Device Recall: Convenience kits MYRINGOTOMY PACK-LF DYNJ59097A
Medline Industries, LP · July 31, 2026
Reason for Recall
Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used.
Distribution
US Nationwide distribution in states of Arkansas, Florida, North Carolina, Maryland, and Texas.
States Affected
NATIONWIDE
Quantity Affected
60
Source: FDA (openFDA Device Enforcement)
Recall number: Z-3209-2026
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.