Recall Z-0350-2025— MEDLINE INDUSTRIES, LP - Northfield

Name: FDA recall Z-0350-2025
Creator: U.S. Food and Drug Administration
Published: 2024-10-04

Class II · Ongoing

Class II FDA medical device recall by MEDLINE INDUSTRIES, LP - Northfield, initiated 2024-10-04. FDA's recall record names no specific 510(k) clearance for this event. Product: ARTHROSCOPY Convenience kit used for surgical procedures, SKU SYNJ910004C. Reason: Products within a Medline pack may be impacted by a packaging error in which an incomplete seal has formed on the packaging thereby creating a packaging seal gap..

Recalling firm: MEDLINE INDUSTRIES, LP - Northfield
Classification: Class II
Status: Ongoing
Initiated: 2024-10-04
Firm location: Northfield, IL, United States

Product description

ARTHROSCOPY Convenience kit used for surgical procedures, SKU SYNJ910004C

Reason for recall

Products within a Medline pack may be impacted by a packaging error in which an incomplete seal has formed on the packaging thereby creating a packaging seal gap.

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