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Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables recalls Safety-Deluxe Lumbar Puncture Tray, Catalog # 975 Product Usage: Surgical procedure
Recalled February 14, 2018 · FDA recall Z-0542-2018 · Robert Busse & Co. Inc.
Hazard
BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose polyprophylene foreign matter above release specification. · FDA Class II
Units
82 cases
Sold at
US Nationwide Distribution
Description
BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose polyprophylene foreign matter above release specification.
Product
Safety-Deluxe Lumbar Puncture Tray, Catalog # 975 Product Usage: Surgical procedure
Manufacturer(s)
Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →