PlainRecalls
FDA Devices Moderate Class II Ongoing

Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, White REF H938671100

Reported: August 31, 2022 Initiated: July 22, 2022 #Z-1577-2022

Product Description

Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, White REF H938671100

Reason for Recall

There is a potential of the packaging not maintaining a sterile barrier for the tip caps.

Details

Units Affected
10140 units
Distribution
Worldwide distribution: US (nationwide) distribution and OUS (foreign) : Australia, Finland, Germany, Spain and United Kingdom.
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, White REF H938671100. Recalled by Baxter Healthcare Corporation. Units affected: 10140 units.
Why was this product recalled?
There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 31, 2022. Severity: Moderate. Recall number: Z-1577-2022.