Robert Busse And D B A Busse Hospital Disposables recalls
Robert Busse And D B A Busse Hospital Disposables appears in 10 official U.S. recall notices indexed by RecallRadar, most recently on 2018-02-14.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 10 |
|---|---|
| Published | 2016-12-28 to 2018-02-14 |
| By agency | FDA Device (10) |
| By classification | Class II (10) |
| By status | terminated (10) |
| Distribution named in notices | FL, PA, US, VA |
Recalls
- Lumbar Puncture Tray, Catalog # 1862 Product Usage: Surgical procedure
FDA Device · Class II · 2018-02-14 · Robert Busse And D B A Busse Hospital Disposables
Reason: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose polyprophylene foreign matter above release specification. - Safety-Deluxe Lumbar Puncture Tray, Catalog # 974 Product Usage: Surgical procedure
FDA Device · Class II · 2018-02-14 · Robert Busse And D B A Busse Hospital Disposables
Reason: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose polyprophylene foreign matter above release specification. - Safety-Deluxe Basic Soft Tissue Biopsy Tray without Biopsy Needle, Catalog # 977 Product Usage: Surgical procedure
FDA Device · Class II · 2018-02-14 · Robert Busse And D B A Busse Hospital Disposables
Reason: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose polyprophylene foreign matter above release specification. - Safety Deluxe Bone Marrow Biopsy/Aspiration Tray, Catalog # 986 Product Usage: Surgical procedure
FDA Device · Class II · 2018-02-14 · Robert Busse And D B A Busse Hospital Disposables
Reason: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose polyprophylene foreign matter above release specification. - Safety Deluxe Bone Marrow Biopsy/ Aspiration Tray with Biopsy Needle and Aspiration Needle Sterile, Catalog # 985 Product Usage: Surgical p…
FDA Device · Class II · 2018-02-14 · Robert Busse And D B A Busse Hospital Disposables
Reason: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose polyprophylene foreign matter above release specification. - Laceration Tray, Catalog # 1892R1 Product Usage: Surgical procedure
FDA Device · Class II · 2018-02-14 · Robert Busse And D B A Busse Hospital Disposables
Reason: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose polyprophylene foreign matter above release specification. - Safety-Deluxe Lumbar Puncture Tray, Catalog # 975 Product Usage: Surgical procedure
FDA Device · Class II · 2018-02-14 · Robert Busse And D B A Busse Hospital Disposables
Reason: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose polyprophylene foreign matter above release specification. - BREAST PACK, Surgical Instrument Tray, REF/Catalog No. 5406, STERILE, Rx Only -- busse Hospital Disposables Hauppauge, NY --- Device Listin…
FDA Device · Class II · 2016-12-28 · Robert Busse And D B A Busse Hospital Disposables
Reason: Covidien issued a labeling update for the Covidien Devon Light Gloves. Busse had incorporated the affected gloves in several kits and distributed them prior to receipt of the recall notification. - SET UP PACK Surgical Instrument Tray, REF/Catalog No. 6250R1, STERILE, Rx Only --- busse Hospital Disposables Hauppauge, NY --- Device List…
FDA Device · Class II · 2016-12-28 · Robert Busse And D B A Busse Hospital Disposables
Reason: Covidien issued a labeling update for the Covidien Devon Light Gloves. Busse had incorporated the affected gloves in several kits and distributed them prior to receipt of the recall notification. - CARPAL TUNNEL PACK, Surgical Instrument Tray, REF/Catalog No. 3366, STERILE, Rx Only -- busse Hospital Disposables Hauppauge, NY --- Device…
FDA Device · Class II · 2016-12-28 · Robert Busse And D B A Busse Hospital Disposables
Reason: Covidien issued a labeling update for the Covidien Devon Light Gloves. Busse had incorporated the affected gloves in several kits and distributed them prior to receipt of the recall notification.