PlainRecalls
FDA Devices Moderate Class II Terminated

Maintenance Flush Kit/Blood Draw Product Code: DT19335

Reported: November 6, 2019 Initiated: July 15, 2019 #Z-0254-2020

Product Description

Maintenance Flush Kit/Blood Draw Product Code: DT19335

Reason for Recall

Supplier initiated recall of the GRIPPER Needles

Details

Units Affected
240 kits
Distribution
IL
Location
Williamston, MI

Frequently Asked Questions

What product was recalled?
Maintenance Flush Kit/Blood Draw Product Code: DT19335. Recalled by Centurion Medical Products Corporation. Units affected: 240 kits.
Why was this product recalled?
Supplier initiated recall of the GRIPPER Needles
Which agency issued this recall?
This recall was issued by the FDA Devices on November 6, 2019. Severity: Moderate. Recall number: Z-0254-2020.