Hauppauge, NY, United States
Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables recalls
1 recall recorded since 2018, most recently on 27 June 2017. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 27 June 2017
- Terminated
- 27 July 2020
- Reason
- BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose polyprophylene foreign matter above release specification.
- Distribution
- US Nationwide Distribution
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-0546-2018, Z-0540-2018, Z-0545-2018, Z-0541-2018, Z-0543-2018, Z-0542-2018, Z-0544-2018
- Safety Deluxe Bone Marrow Biopsy/Aspiration Tray, Catalog # 986 Product Usage: Surgical procedure
- Safety-Deluxe Lumbar Puncture Tray, Catalog # 974 Product Usage: Surgical procedure
- Lumbar Puncture Tray, Catalog # 1862 Product Usage: Surgical procedure
- Safety-Deluxe Basic Soft Tissue Biopsy Tray without Biopsy Needle, Catalog # 977 Product Usage: Surgical procedure
- Safety Deluxe Bone Marrow Biopsy/ Aspiration Tray with Biopsy Needle and Aspiration Needle Sterile, Catalog # 985 Product Usage: Surgical procedure
- Safety-Deluxe Lumbar Puncture Tray, Catalog # 975 Product Usage: Surgical procedure
- Laceration Tray, Catalog # 1892R1 Product Usage: Surgical procedure
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.