Recall Z-0253-2020— Centurion Medical Products Corporation

Name: FDA recall Z-0253-2020
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. It names one FDA 510(k) clearance: K021999. Product: Port full Access Tray Product Code: DT19330. 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

510(k) clearances named in this recall

1 on FDA's record

K021999 — GRIPPER PLUS NEEDLEDeltec, Inc.·cleared 2002-08-13

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

Port full Access Tray Product Code: DT19330

Reason for recall

Supplier initiated recall of the GRIPPER Needles

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