FDA Enforcement Class II Terminated

Lumbar Puncture Tray, Catalog # 1862 Product Usage: Surgical procedure

Recall: Z-0545-2018 · Reported February 14, 2018

Enforcement

Recall Number
Z-0545-2018
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

Lumbar Puncture Tray, Catalog # 1862 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) 1710206/Expiration Date: 05/30/2022; 2) 1710040/Expiration Date: 01/30/2022; 3) 1610536/Expiration Date: 12/30/2021; 4) 1610423/No Expiration Date; 5) 1610351/No Expiration Date; 6) 1610219/No Expiration Date; 7) 1610090/No Expiration Date

Distribution

US Nationwide Distribution

Quantity

1037 in total