FDA Enforcement Class II Terminated

Safety-Deluxe Lumbar Puncture Tray, Catalog # 975 Product Usage: Surgical procedure

Recall: Z-0542-2018 · Reported February 14, 2018

Enforcement

Recall Number
Z-0542-2018
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 # 975 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 Numbers/Expiration Dates: 1) 1610197/Expiration Date: 12/01/2018; 2) 1610204/Expiration Date: 02/01/2019; 3) 1610075/Expiration Date: 06/01/2018; 4) 1610431/Expiration Date: 05/30/2019; 5) 1610246/Expiration Date: 02/01/2019; 6) 1610204/Expiration Date: 02/01/2019

Distribution

US Nationwide Distribution

Quantity

82 cases