Class II

Medical Device Recall: Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A

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

341

Source: FDA (openFDA Device Enforcement)

Recall number: Z-3207-2026

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.