Recall Z-0256-2020— Centurion Medical Products Corporation

Name: FDA recall Z-0256-2020
Creator: U.S. Food and Drug Administration
Published: 2019-07-15

Class II · Terminated

Class II FDA medical device recall by Centurion Medical Products Corporation, initiated 2019-07-15, terminated 2020-08-31. FDA's recall record names no specific 510(k) clearance for this event. Product: PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817. Reason: Supplier initiated recall of the GRIPPER Needles.

Recalling firm: Centurion Medical Products Corporation
Classification: Class II
Status: Terminated
Initiated: 2019-07-15
Terminated: 2020-08-31
Firm location: Williamston, MI, United States

Product description

PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817

Reason for recall

Supplier initiated recall of the GRIPPER Needles

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