Health product recall

30 atm MONARCH® Inflation Syringe

Last updated

Summary

Product
30 atm MONARCH® Inflation Syringe
Issue
Medical devices - Labelling and packaging
Medical devices - Sterility
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

30 atm MONARCH® Inflation Syringe

More than 10 numbers, contact manufacturer.

IN2130/B
IN2130

Issue

On July 31, 2024, Merit internally identified an issue related to potential holes being found in the Tyvek® sterile barrier of certain MONARCH® inflation devices during the manufacture of lot H3003824. Visual inspection of the packaged units from lot H3003824 found a potential hole in 28 of 776 manufactured units. The 28 units underwent a bubble test where 23 of the 28 units failed, confirming a hole in the sterile barrier.  Further investigation has determined that certain placements of the MONARCH® inflation device within a rigid formed blister tray can cause a hole in the Tyvek®. Should a MONARCH® inflation device's placement result in the unit's retainer cap being positioned above the rigid blister flange, the Tyvek® can contact a multivac's cross-cut station potentially leading to an abrasion or hole in the Tyvek®.

Recall start date: August 28, 2024

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies

Merit Medical Systems Inc.

1600 West Merit Parkway, South Jordan, Utah, United States, 84095

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-76013

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