PlainRecalls
FDA Devices Critical Class I Ongoing

stay-safe /Luer Catheter Ext. 6 in

Reported: April 3, 2024 Initiated: January 23, 2024 #Z-1327-2024

Product Description

stay-safe /Luer Catheter Ext. 6 in

Reason for Recall

The peroxide cross-linked tubing has leachables identified as NDL PCBAs.

Details

Units Affected
105,700 eaches
Distribution
Domestic: Nationwide Distribution.
Location
Waltham, MA

Frequently Asked Questions

What product was recalled?
stay-safe /Luer Catheter Ext. 6 in. Recalled by Fresenius Medical Care Holdings, Inc.. Units affected: 105,700 eaches.
Why was this product recalled?
The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 3, 2024. Severity: Critical. Recall number: Z-1327-2024.