Home › Companies › Bard Peripheral Vascular Inc.

Recall company profile

Bard Peripheral Vascular Inc. Recalls

Overview of recall records associated with Bard Peripheral Vascular Inc., including dates, categories and classifications where available.

100recall records

Feb 25, 2026latest record date

May 23, 2018earliest record date

Recall history in this database

Classification mix: Class II: 99, Class I: 1.

Medical DeviceSep 4, 2019

Bard Peripheral Vascular GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet recall — FDA Z-2390-2019

The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceSep 4, 2019

Bard Peripheral Vascular GlidePath Long-Term Hemodialysis Catheter, REF/Product recall — FDA Z-2389-2019

The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceSep 4, 2019

Bard Peripheral Vascular EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet recall — FDA Z-2372-2019

The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceSep 4, 2019

Bard Peripheral Vascular GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet recall — FDA Z-2391-2019

The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceSep 4, 2019

Bard Peripheral Vascular EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product recall — FDA Z-2368-2019

The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceSep 4, 2019

Bard Peripheral Vascular GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet recall — FDA Z-2395-2019

The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceSep 4, 2019

Bard Peripheral Vascular EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded recall — FDA Z-2382-2019

The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceSep 4, 2019

Bard Peripheral Vascular GlidePath Long-Term Hemodialysis Catheter, REF/Product recall — FDA Z-2388-2019

The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceSep 4, 2019

Bard Peripheral Vascular EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product recall — FDA Z-2369-2019

The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceSep 4, 2019

Bard Peripheral Vascular EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded recall — FDA Z-2377-2019

The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceSep 4, 2019

Bard Peripheral Vascular EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet recall — FDA Z-2375-2019

The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceSep 4, 2019

Bard Peripheral Vascular GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet recall — FDA Z-2383-2019

The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceSep 4, 2019

Bard Peripheral Vascular EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded recall — FDA Z-2379-2019

The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceSep 4, 2019

Bard Peripheral Vascular EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded recall — FDA Z-2378-2019

The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceSep 4, 2019

Bard Peripheral Vascular EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet recall — FDA Z-2371-2019

The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceSep 4, 2019

Bard Peripheral Vascular EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet recall — FDA Z-2373-2019

The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceSep 4, 2019

Bard Peripheral Vascular EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded recall — FDA Z-2381-2019

The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceSep 4, 2019

Bard Peripheral Vascular EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product recall — FDA Z-2370-2019

The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceSep 4, 2019

Bard Peripheral Vascular GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet recall — FDA Z-2384-2019

The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceAug 14, 2019

Bard Peripheral Vascular EnCor Breast Biopsy Probes, packaged individually in sterile recall — FDA Z-2213-2019

There has been an increase in complaints related to leaks, suction issues, and failure to obtain samples while using the product.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceAug 14, 2019

Bard Peripheral Vascular EnCor Breast Biopsy Probes, packaged individually in sterile recall — FDA Z-2214-2019

There has been an increase in complaints related to leaks, suction issues, and failure to obtain samples while using the product.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceAug 14, 2019

Bard Peripheral Vascular EnCor Breast Biopsy Probes, packaged individually in sterile recall — FDA Z-2211-2019

There has been an increase in complaints related to leaks, suction issues, and failure to obtain samples while using the product.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceAug 14, 2019

Bard Peripheral Vascular EnCor Breast Biopsy Probes, packaged individually in sterile recall — FDA Z-2212-2019

There has been an increase in complaints related to leaks, suction issues, and failure to obtain samples while using the product.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Medical DeviceAug 14, 2019

Bard Peripheral Vascular EnCor Breast Biopsy Probes, packaged individually in sterile recall — FDA Z-2209-2019

There has been an increase in complaints related to leaks, suction issues, and failure to obtain samples while using the product.

Class IIFDA: TerminatedBard Peripheral Vascular Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Bard Peripheral Vascular Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.