Bard Peripheral Vascular recalls
Bard Peripheral Vascular has 138 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 25 Feb 2026. 35 are still ongoing. 3 were reported in the last 12 months. The most frequent reason is device malfunction.
Total recalls138since 2013
Last 12 months3reported
Class I54% of total
Ongoing35latest 25 Feb 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 5 4%Class II 133 96%Class III 0 0%
Why bard peripheral vascular is recalled
Product types
By year
Ongoing bard peripheral vascular recalls
35 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Broviac Single-Lumen CV Catheter Cutdown Tray recalled | Bard Peripheral Vascular | Sterility | Nationwide |
| Device | CLASS II | Safe-T-Centesis Catheter Drainage Tray recalled | Bard Peripheral Vascular | Lead & Heavy Metals | Nationwide |
| Device | CLASS II | Venclose digiRF Generators recalled by Bard Peripheral Vascular | Bard Peripheral Vascular | Temperature Abuse | Nationwide |
| Device | CLASS I | Rotarex Atherectomy System and Instructions for Use recalled | Bard Peripheral Vascular | Lead & Heavy Metals | Nationwide |
| Device | CLASS II | Bard Marquee Disposable Core Biopsy Instrument Kit: Bard Marquee Kit recalled | Bard Peripheral Vascular | Lead & Heavy Metals | Nationwide |
| Device | CLASS II | The Evsrf catheter is a sterile recalled by Bard Peripheral Vascular | Bard Peripheral Vascular | Lead & Heavy Metals | Nationwide |
All bard peripheral vascular recalls, newest first
138 totalAbout this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.