Home › CAREFUSION 2200, INC › N/A
N/A
CAREFUSION 2200, INC · Model 4380 · UDI-DI 10885403108563
FSH
Prescription
8
510(k) clearances
68
Adverse events (4 deaths)
7
Recalls
22
Facilities
Description
Economy Soft Tissue Biopsy Tray
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-05-21 | Bard Access Systems, Inc. | Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier. |
| 2024-04-08 | MEDLINE INDUSTRIES, LP - Northfield | Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that ma |
| 2017-02-23 | Carefusion 2200 Inc | The integrity of the sterile packaging is potentially compromised. |
| 2017-02-23 | Carefusion 2200 Inc | The integrity of the sterile packaging is potentially compromised. |
| 2017-02-23 | Carefusion 2200 Inc | The integrity of the sterile packaging is potentially compromised. |
| 2017-02-23 | Carefusion 2200 Inc | The integrity of the sterile packaging is potentially compromised. |
| 2017-02-23 | Carefusion 2200 Inc | The integrity of the sterile packaging is potentially compromised. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.