Home › Bard Peripheral Vascular, Inc. › BARD® PARSONNET
BARD® PARSONNET
Bard Peripheral Vascular, Inc. · Model 007604 · UDI-DI 00801741089985
DWP
Prescription
10
510(k) clearances
171
Adverse events
1
Recalls
44
Facilities
Description
BARD® PARSONNET™ Vascular Probe 1.5 mm x 45 cm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-12-06 | Baxter Healthcare Corporation | Cardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align with some of the produ |
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.