Class I — Serious Health Hazard

Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 Recalled by TELEFLEX-MORRISVILLE Due to Device vented gas below the stated pressure.

Date: June 14, 2019
Company: TELEFLEX-MORRISVILLE
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 TELEFLEX-MORRISVILLE directly.

Affected Products

Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 for use with ventilators.

Quantity: 9,312 each

Why Was This Recalled?

Device vented gas below the stated pressure.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About TELEFLEX-MORRISVILLE

TELEFLEX-MORRISVILLE has 1 total recall tracked by RecallDetector.

Related Recalls

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