PlainRecalls
FDA Devices Moderate Class II Ongoing

Refer to RES

Reported: April 23, 2025 Initiated: March 3, 2025 #Z-1618-2025

Product Description

Refer to RES

Reason for Recall

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Details

Units Affected
11889 units
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.
Location
Northfield, IL

Frequently Asked Questions

What product was recalled?
Refer to RES. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 11889 units.
Why was this product recalled?
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 23, 2025. Severity: Moderate. Recall number: Z-1618-2025.