Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Bard Caliber (CL3030) Inflation Device Product Usage: Inflation Device intended Recalled by PEROUSE MEDICAL Due to Additional instructions for use due to inability to...

Date: October 6, 2014
Company: PEROUSE MEDICAL
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact PEROUSE MEDICAL directly.

Affected Products

Bard Caliber (CL3030) Inflation Device Product Usage: Inflation Device intended for use during cardiovascular to create and maintain, monitor pressure in the balloon catheter - balloon inflation device for angioplasty procedures

Quantity: 24821 units

Why Was This Recalled?

Additional instructions for use due to inability to raise the pressure above 10 atm during inflation phase may result in an incomplete inflation or delay in procedure

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About PEROUSE MEDICAL

PEROUSE MEDICAL has 3 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report