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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 141–160 of 232 recalls

Bard Peripheral Vascular Inc: EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product C...

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.

FDAMay 31, 2019AL, AK, AZ +49 more• Bard Peripheral Vascular Inc

Bard Peripheral Vascular Inc: EQUISTREAM XK Long-Term Hemodialysis Catheter with Prelo...

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.

FDAMay 31, 2019AL, AK, AZ +49 more• Bard Peripheral Vascular Inc

Bard Peripheral Vascular Inc: GlidePath Long-Term Hemodialysis Catheter with Preloaded ...

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.

FDA

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May 31, 2019

AL, AK, AZ +49 more

• Bard Peripheral Vascular Inc

Bard Peripheral Vascular Inc: EnCor Breast Biopsy Probes, packaged individually in ster...

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

FDAMay 2, 2019Nationwide• Bard Peripheral Vascular Inc

Smith & Nephew, Inc.: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT, SIZE 4, LE...

The stem taper on this device is undersized; the gauge point is not deep enough.

Class IIModerate

FDANov 4, 2014Nationwide• Smith & Nephew, Inc.

Smith & Nephew, Inc.: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT, SIZE 5, RI...

The stem taper on this device is undersized; the gauge point is not deep enough.

Class IIModerate

FDANov 4, 2014Nationwide• Smith & Nephew, Inc.

Smith & Nephew, Inc.: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT, SIZE 6, LE...

The stem taper on this device is undersized; the gauge point is not deep enough.

Class IIModerate

FDANov 4, 2014Nationwide• Smith & Nephew, Inc.

Bard Peripheral Vascular Inc: Bard DuaLok Breast Lesion Localization Wire, Product Co...

Bard Peripheral is recalling the Bard DuaLok Breast Lesion Localization Wire because it may be at risk of having portions of the wire protruding from the packaging, thus representing a breach of sterile barrier.

Class IIModerate

FDAAug 26, 2014Nationwide• Bard Peripheral Vascular Inc

Smith & Nephew, Inc.: RENASYS EZ Negative Pressure Wound Therapy (NPWT) System ...

Modification were made to the RENASYS EZ NPWT Systems without a 510(k) or PreMarket Approval notification.

Class IIModerate

FDAAug 13, 2014Nationwide• Smith & Nephew, Inc.

Smith & Nephew, Inc.: RENASYS EZ/ RENASYS EZ Plus 800 mL canister with Solidifi...

RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet port on the canister lid.

Class IIModerate

FDAJul 18, 2014Nationwide• Smith & Nephew, Inc.

Smith & Nephew, Inc.: RENASYS EZ/ RENASYS EZ Plus 250 mL canister with Solidifi...

RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet port on the canister lid.

Class IIModerate

FDAJul 18, 2014Nationwide• Smith & Nephew, Inc.

Smith & Nephew, Inc.: RENASYS EZ/ RENASYS EZ Plus 800 mL canister (w/o CLP) wit...

RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet port on the canister lid.

Class IIModerate

FDAJul 18, 2014Nationwide• Smith & Nephew, Inc.

Bard Peripheral Vascular Inc: Bard Magnum Disposable Biopsy Core Needle 16 gauge, Catal...

The recall was initiated after the firm determined that some Magnum Disposable Biopsy Core Needle 16 gauge lots may exhibit an exposed sample chamber, due to extended stylet length resulting from a loose hub connection. The exposed sample chamber will typically result in an inability to obtain the biopsy sample. In the majority of reported cases, there was no injury to the patient or user. When us

FDAOct 8, 2009Nationwide• Bard Peripheral Vascular Inc

Bard Peripheral Vascular Inc: Bard Magnum Disposable Biopsy Core Needle 16 gauge, Catal...

FDAOct 8, 2009Nationwide• Bard Peripheral Vascular Inc

Bard Peripheral Vascular Inc: Bard Magnum Disposable Biopsy Core Needle 16 gauge, Catal...

FDAOct 8, 2009Nationwide• Bard Peripheral Vascular Inc

Bard Peripheral Vascular Inc: Bard Magnum Disposable Biopsy Core Needle 16 gauge, Catal...

FDAOct 8, 2009Nationwide• Bard Peripheral Vascular Inc

Smith & Nephew, Inc., Endoscopy Div.: AIMER ENDOFEMORAL 6MM OFFSET (GREEN) Part Number 72201716...

Device may have improper Laser Marking, 4mm device may be marked as 6mm and 6mm device may be marked as 4mm.

FDASep 3, 2009Nationwide• Smith & Nephew, Inc., Endoscopy Div.

Smith & Nephew, Inc., Endoscopy Div.: AlMER ENDOFEMORAL 4MM OFFSET (PURPLE) Part Number 7220171...

Device may have improper Laser Marking, 4mm device may be marked as 6mm and 6mm device may be marked as 4mm.

FDASep 3, 2009Nationwide• Smith & Nephew, Inc., Endoscopy Div.

Smith & Nephew, Inc., Endoscopy Div.: AIMER ENDOFEMORAL 6MM OFFSET (GREEN) Part Number 72201716...

Device may have improper Laser Marking, 4mm device may be marked as 6mm and 6mm device may be marked as 4mm.

FDASep 3, 2009Nationwide• Smith & Nephew, Inc., Endoscopy Div.

Smith & Nephew Inc: Exogen 4000+ Ultrasound Bone Healing System, SAFHS, Part ...

Problems with transducer may result in a reduced ultrasound output.

FDAJun 5, 2009Nationwide• Smith & Nephew Inc