Recall Z-0922-2026— Medline Industries, LP

Name: FDA recall Z-0922-2026
Creator: U.S. Food and Drug Administration
Published: 2025-11-13

Class II · Ongoing

Class II FDA medical device recall by Medline Industries, LP, initiated 2025-11-13. FDA's recall record names no specific 510(k) clearance for this event. Product: FORCEP, STD STR, STERILE KELLY, 5.5 IN, Item Number DYNJ04048. Reason: 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..

Recalling firm: Medline Industries, LP
Classification: Class II
Status: Ongoing
Initiated: 2025-11-13
Firm location: Northfield, IL, United States

Product description

FORCEP, STD STR, STERILE KELLY, 5.5 IN, Item Number DYNJ04048

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.