Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Pneupac paraPac plus 300 ventilator kit Recalled by Smiths Medical ASD Inc. Due to Two devices were labeled with the same serial...

Date: July 15, 2021
Company: Smiths Medical ASD Inc.
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 Smiths Medical ASD Inc. directly.

Affected Products

Pneupac paraPac plus 300 ventilator kit, REF P300NGB

Quantity: 2 units

Why Was This Recalled?

Two devices were labeled with the same serial number

Where Was This Sold?

UK

About Smiths Medical ASD Inc.

Smiths Medical ASD Inc. has 169 total recalls tracked by RecallDetector.

Related Recalls

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