Recall Z-0510-2026— Medline Industries, LP

Name: FDA recall Z-0510-2026
Creator: U.S. Food and Drug Administration
Published: 2025-10-03

Class II · Ongoing

Class II FDA medical device recall by Medline Industries, LP, initiated 2025-10-03. FDA's recall record names no specific 510(k) clearance for this event. Product: MEDLINE STERILE BASIC EYE PACK 16: 1) REF: DYNJ37743D; 2) REF: DYNJ37743F.. Reason: Medline has identified specific sterile eye procedure kits with pouch packaging that may exhibit open seals..

Recalling firm: Medline Industries, LP
Classification: Class II
Status: Ongoing
Initiated: 2025-10-03
Firm location: Northfield, IL, United States

Product description

MEDLINE STERILE BASIC EYE PACK 16: 1) REF: DYNJ37743D; 2) REF: DYNJ37743F.

Reason for recall

Medline has identified specific sterile eye procedure kits with pouch packaging that may exhibit open seals.

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