Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables: Medical Device Recall in 2018 - (Recall #: Z-0544-2018)

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:

Laceration Tray, Catalog # 1892R1 Product Usage: Surgical procedure

Product Classification:

Class II

Date Initiated: June 27, 2017

Date Posted: February 14, 2018

Recall Number: Z-0544-2018

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: 75 cases

Code Information:

Lot Numbers/Expiration Dates: 1) 1730650/Expiration Date: 10/30/2021; 2) 1630921/Expiration Date: 11/02/2020; 3) 1631124/Expiration Date: 10/30/2020; 4) 1631386/Expiration Date: 05/30/2021; 5) 1631679/Expiration Date: 05/30/2021

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated