Recall Z-1683-2022— Medline Industries Inc.

Name: FDA recall Z-1683-2022
Creator: U.S. Food and Drug Administration
Published: 2022-07-21

Class II · Ongoing

Class II FDA medical device recall by Medline Industries Inc., initiated 2022-07-21. FDA's recall record names no specific 510(k) clearance for this event. Product: Medline CHEST TUBE REORDER NO: DYNJ36762A. Reason: Due to a non-sterile component (tape) being place within the sterile portion of the Chest Tube Convenience Kit.

Recalling firm: Medline Industries Inc.
Classification: Class II
Status: Ongoing
Initiated: 2022-07-21
Firm location: Laredo, TX, United States

Product description

Medline CHEST TUBE REORDER NO: DYNJ36762A

Reason for recall

Due to a non-sterile component (tape) being place within the sterile portion of the Chest Tube Convenience Kit

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