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U.S. Department of Health and Human Services

Class 2 Device Recall Lumbar Puncture Tray

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 Class 2 Device Recall Lumbar Puncture Traysee related information
Date Initiated by FirmJune 27, 2017
Create DateFebruary 07, 2018
Recall Status1 Terminated 3 on July 27, 2020
Recall NumberZ-0545-2018
Recall Event ID 78950
510(K)NumberK032432 K110883 
Product Classification Lumbar puncture tray (adult & pediatric) - Product Code PWY
ProductLumbar Puncture Tray, Catalog # 1862 Product Usage: Surgical procedure
Code Information 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
Recalling Firm/
Manufacturer		 Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables
75 Arkay Dr
Hauppauge NY 11788-3707
Manufacturer Reason
for Recall		BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose polyprophylene foreign matter above release specification.
FDA Determined
Cause 2		Nonconforming Material/Component
ActionOn June 27, 2017, Busse Hospital Disposables distributed Urgent Medical Device Recall notices and Response Forms to their customers via courier service. A copy of the supplier's recall notice was also provided to customers. Customers were advised to conduct the following: " Discontinue use of needle immediately. " Please check your inventory and cease distribution immediately. " If you have distributed the above products, please contact your customers and inform them of this recall immediately. " Contact Busse Hospital Disposables for a Return Good Authorization number. " Complete and Return the Response Form via fax to 631-435-2849 or via email to: ijacobo@busseinc.com. Customers with questions may call 631-435-4711, ext. 254.
Quantity in Commerce1037 in total
DistributionUS Nationwide Distribution
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database510(K)s with Product Code = PWY
510(K)s with Product Code = PWY
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