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Bard Peripheral Vascular Inc

Bard Peripheral Vascular Inc Recalls

All product recalls associated with Bard Peripheral Vascular Inc.

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Recall Summary

Total Recalls

232

Past Year

Class I (Serious)

Most Recent

Nov 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 61–80 of 232 recalls

Bard Marquee Biopsy Instrument (Bard) – Depth Switch Detachment (2021)

Due to the Penetration Depth Switch used to select the desired penetration depth of the biopsy needle for soft tissue biopsies, detaches from the device during use.

FDAJan 14, 2021AL, AK, AZ +49 more• Bard Peripheral Vascular Inc

VERSABOND AB Bone Cement (Smith & Nephew) – Consistency Problem (2020)

Potential heat and humidity exposure. The affected lot contained an atypical sandy, flaky or grainy consistency when mixing.

FDADec 18, 2020Nationwide• Smith & Nephew, Inc.

VENOVO Venous Stent 8F (Bard) – Deployment Expansion Issue (2020)

Reports of the proximal end of the stent not immediately expanding upon deployment and remaining connected to the delivery system.

FDADec 14, 2020Nationwide

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• Bard Peripheral Vascular Inc

VENOVO Venous Stent 9F (Bard) – Deployment Expansion Issue (2020)

Reports of the proximal end of the stent not immediately expanding upon deployment and remaining connected to the delivery system.

FDADec 14, 2020Nationwide• Bard Peripheral Vascular Inc

VENOVO Venous Stent 10F (Bard) – Deployment Expansion Issue (2020)

Reports of the proximal end of the stent not immediately expanding upon deployment and remaining connected to the delivery system.

FDADec 14, 2020Nationwide• Bard Peripheral Vascular Inc

Trigen Intertan Nail (Smith & Nephew) – Packaging Error (2020)

Manufacturing packaging error.

FDANov 2, 2020Nationwide• Smith & Nephew, Inc.

Bard Conquest PTA Balloon (Bard) – Incorrect Balloon Size (2020)

Dilation catheter packaged with the wrong size balloon. The labeling states that the balloon size is 6mm x 40mm, however included is a 5mm x 40mm balloon. Use of a balloon that has a smaller diameter than expected could result in inconsequential prolongation of an existing procedure.

FDAOct 1, 2020Nationwide• Bard Peripheral Vascular Inc

Genesis (Smith & Nephew) – locking detail defect (2020)

The anterior locking detail does not meet its design specifications.

FDASep 21, 2020Nationwide• Smith & Nephew, Inc.

Arthrogarde Hip Access Cannula (Smith & Nephew) – locking feature defect (2020)

The J Lock feature on the cannula body was manufactured incorrectly, preventing the cannula from locking into an irrigation extender or arthroscope in the correct orientation.

FDASep 21, 2020CA, CO, CT +17 more• Smith & Nephew, Inc.