Recall Z-2081-2020— Becton Dickinson & Company

Name: FDA recall Z-2081-2020
Creator: U.S. Food and Drug Administration
Published: 2020-02-26

Class II · Terminated

Class II FDA medical device recall by Becton Dickinson & Company, initiated 2020-02-26, terminated 2020-09-22. It names one FDA 510(k) clearance: K102159. Product: BARD MYPICC KIT 4F Dual-Lumen, Catalog Number CK000418B. Reason: The kits contain surgical gowns which were subject to a recall by the supplier..

Recalling firm: Becton Dickinson & Company
Classification: Class II
Status: Terminated
Initiated: 2020-02-26
Terminated: 2020-09-22
Firm location: Franklin Lakes, NJ, United States

510(k) clearances named in this recall

1 on FDA's record

K102159 — POWERPICC SV CATHETERSC.R. Bard, Inc.·cleared 2010-11-17

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

BARD MYPICC KIT 4F Dual-Lumen, Catalog Number CK000418B

Reason for recall

The kits contain surgical gowns which were subject to a recall by the supplier.

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