Class II

Medical Device Recall: FORCEP, STD STR, STERILE KELLY, 5.5 IN, Item Number DYNJ04048

Medline Industries, LP · November 13, 2025

Reason for Recall

The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.

Distribution

US Nationwide distribution in the states CA, CO, IL, KS, and MI.

States Affected

NATIONWIDE

Quantity Affected

53 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0922-2026

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.