Recall Z-0533-2024— MEDLINE INDUSTRIES, LP - Northfield

Class II · Ongoing

Class II FDA medical device recall by MEDLINE INDUSTRIES, LP - Northfield, initiated 2023-10-19. FDA's recall record names no specific 510(k) clearance for this event. Product: Medline Leg bag, REF DYND12574. Reason: Undeclared latex.

Recalling firm
MEDLINE INDUSTRIES, LP - Northfield
Classification
Class II
Status
Ongoing
Initiated
2023-10-19
Firm location
Northfield, IL, United States

Product description

Medline Leg bag, REF DYND12574

Reason for recall

Undeclared latex

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