PlainRecalls
FDA Devices Moderate Class II Terminated

Kit, Port Access Product Code: DYNDC1582A

Reported: November 6, 2019 Initiated: July 15, 2019 #Z-0255-2020

Product Description

Kit, Port Access Product Code: DYNDC1582A

Reason for Recall

Supplier initiated recall of the GRIPPER Needles

Details

Units Affected
11260 kits
Distribution
IL
Location
Williamston, MI

Frequently Asked Questions

What product was recalled?
Kit, Port Access Product Code: DYNDC1582A. Recalled by Centurion Medical Products Corporation. Units affected: 11260 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-0255-2020.