Bard Peripheral Vascular recalls
Bard Peripheral Vascular has 139 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 7 Oct 2026. 36 are still ongoing. 3 were reported in the last 12 months.
Total recalls139since 2013
Last 12 months3reported
Class I54% of total
Ongoing36latest 7 Oct 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 5 4%Class II 134 96%Class III 0 0%
Why bard peripheral vascular is recalled
Product types
By year
Ongoing bard peripheral vascular recalls
36 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | EnCor EnCompass Breast Biopsy and Tissue Removal System Console recalled | Bard Peripheral Vascular | Device Malfunction | Nationwide |
| Device | CLASS II | Broviac 4. 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 | Other | 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 | Device Malfunction | Nationwide |
| Device | CLASS II | Bard Marquee Disposable Core Biopsy Instrument Kit: Bard Marquee Kit recalled | Bard Peripheral Vascular | Other | Nationwide |
All bard peripheral vascular recalls, newest first
139 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.