Recall Z-3208-2026— Medline Industries, LP

Class II · Ongoing

Class II FDA medical device recall by Medline Industries, LP, initiated 2026-07-31. FDA's recall record names no specific 510(k) clearance for this event. Product: Convenience kits MINOR PACK DYNJ58421A SPRINGHILL MINOR PACK DYNJ40734F. Reason: 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..

Recalling firm
Medline Industries, LP
Classification
Class II
Status
Ongoing
Initiated
2026-07-31
Firm location
Northfield, IL, United States

Product description

Convenience kits MINOR PACK DYNJ58421A SPRINGHILL MINOR PACK DYNJ40734F

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.

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