FDA Recall
Terminated
Maintenance Flush Kit/Blood Draw Product Code: DT19335
Recall: Z-0254-2020
·
Initiated July 15, 2019
Recall
- Recall Number
- Z-0254-2020
- Event Number
- 83542
- Firm
- Centurion Medical Products Corporation
- FEI Number
- 3008403546
- Product Code
- OIB
- Status
- Terminated
- Root Cause
- Nonconforming Material/Component
- Initiated
- July 15, 2019
- Terminated
- August 31, 2020
- Address
- 100 Centurion Way, Williamston, MI, 48895-9086
Description
Maintenance Flush Kit/Blood Draw Product Code: DT19335
Reason
Supplier initiated recall of the GRIPPER Needles
Action
1. Please identify all inventory that you have within your possession and cease use immediately. 2. Complete the enclosed accountability record, whether or not you have product, and fax or email at your earliest convenience to the attention of Lisa Carpenter. Upon receipt of this record, Centurion Representative will contact you regarding retrieval of the product from your facility. 3. Please forward this recall information to any facilities to who this product may have been further distributed, instructing them to cease use immediately.
Distribution
IL
Quantity
240 kits