ProductGuru Recalls

Brand

Bard Peripheral Vascular Inc: official recall notices

5 official recall or safety notices on this site name Bard Peripheral Vascular Inc, dated between 2024-07-10 and 2026-08-20. They were issued by 1 authority: US FDA — Medical Devices (5).

Countries where the notices were issued: United States (5).

Name as written in the notices: Bard Peripheral Vascular Inc. This is the brand or the responsible company as each authority recorded it. A recall shows a safety system working; it is not a verdict on a brand. Follow the official notice for each product.

Notices by year

YearNotices
20261
20251
20243

Notices by authority

AuthorityNotices
US FDA — Medical Devices5

All notices

DateAuthorityProductHazard (as classified)
2026-08-20US FDA — Medical DevicesEnCor EnCompass Breast Biopsy and Tissue Removal System Console (model number: ENCPCONSOLE) and Driver (model number: EN—
2025-02-05US FDA — Medical DevicesRotarex Atherectomy System and Instructions for Use, BD SET Rotarex: S 6 F x 110 cm, REF: 80236; S 6 F x 135 cm, REF:—
2024-09-30US FDA — Medical DevicesBard Marquee Disposable Core Biopsy Instrument Kit: BARD MARQUEE KIT 12G X 10 CM, REF: MQK1210; BARD MARQUEE 12G X 10—
2024-09-04US FDA — Medical DevicesThe EVSRF catheter is a sterile, single-use disposable medical device for endovenous radiofrequency ablation, a procedur—
2024-07-10US FDA — Medical DevicesGuidewire 70cm x 1mm (0.038 ) REF 5583705 These accessories are intended for use with Bard 14.5 Fr. Long-Term Dual Lu—

All brands →