Public recall detail

IMPRA® Carboflo™ Flex Carbon-Lined

2025-03-13

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Recall Safety notice
Quick summary

Quick summary: IMPRA® Carboflo™ Flex Carbon-Lined. Date: 2025-03-13.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: IMPRA® Carboflo™ Flex Carbon-Lined. Date: 2025-03-13.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandBard Peripheral Vascular, Inc.
ProductIMPRA® Carboflo™ Flex Carbon-Lined
IssueMedical devices - Performance
Recall classType II
IdentificationRA-77111

Affected products

ProductIMPRA® Carboflo™ Flex Carbon-Lined
LotVTHV0076
ModelF5010C
Serial numberVTHV0076
DescriptionIMPRA® Carboflo™ Flex Carbon-Lined

Issue

One lot of IMPRA® Carboflo™ Flex 10 mm x 50 cm, product catalog code F5010C, lot number VTHV0076, was discovered to be missing the removable spiral reinforcement material (beading) that should be present on the product. Recall start date: March 4, 2025

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Cardiovascular
CompaniesBard Peripheral Vascular, Inc. 1625 West 3rd Street, Tempe, Arizona, United States, 85281
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-77111
Background{}
CompaniesBard Peripheral Vascular, Inc. 1625 West 3rd Street, Tempe, Arizona, United States, 85281
AudiencesHealthcare
Source updated2025-03-13

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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