FDA Enforcement Class II Terminated

Safety-Deluxe Lumbar Puncture Tray, Catalog # 974 Product Usage: Surgical procedure

Recall: Z-0540-2018 · Reported February 14, 2018

Enforcement

Recall Number
Z-0540-2018
Event ID
78950
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
February 14, 2018
Initiation Date
June 27, 2017
Classification Date
February 6, 2018
Termination Date
July 27, 2020
Address
75 Arkay Dr, N/A, Hauppauge, NY, 11788-3707, United States

Description

Safety-Deluxe Lumbar Puncture Tray, Catalog # 974 Product Usage: Surgical procedure

Reason

BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose polyprophylene foreign matter above release specification.

Code Info

Lot Number/Expiration Date: 1) 1610300/Expiration Date 03/01/2019; 2) 1610503/Expiration Date 05/30/2019; 3) 1710059/Expiration Date: 09/30/2019; 4) 1610383/Expiration Date: 02/28/2019; 5) 1610463/Expiration Date: 05/30/2019; 6) 1610215/Expiration Date: 02/01/2019; 7) 1610114/Expiration Date: 11/01/2018; 8) 1610044/Expiration Date: 06/01/2018;

Distribution

US Nationwide Distribution

Quantity

470 cases