Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables: Medical Device Recall in 2018 - (Recall #: Z-0542-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: June 27, 2017

Date Posted: February 14, 2018

Recall Number: Z-0542-2018

Event ID: 78950

Reason for Recall:

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

Status: Terminated

Product Quantity: 82 cases

Code Information:

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 Pattern:

US Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated