Z-0254-2020 Class II Terminated
FDA device recall Z-0254-2020 was initiated by Centurion Medical Products Corporation on July 15, 2019 and is designated Class II. Reason for recall: Supplier initiated recall of the GRIPPER Needles The recall status is terminated (terminated August 31, 2020). Affected quantity: 240 kits.
Recall Details
- Product Type
- Devices
- Report Date
- November 6, 2019
- Initiation Date
- July 15, 2019
- Termination Date
- August 31, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 240 kits
Product Description
Maintenance Flush Kit/Blood Draw Product Code: DT19335
Reason for Recall
Supplier initiated recall of the GRIPPER Needles
Distribution Pattern
IL
Code Information
Lot Number Expiration 2018110501 7/31/2021 2018121801 7/31/2021 2019013001 9/30/2021 2019032901 9/30/2021