Date Initiated by Firm | July 15, 2019 |
Create Date | October 31, 2019 |
Recall Status1 |
Terminated 3 on August 31, 2020 |
Recall Number | Z-0254-2020 |
Recall Event ID |
83542 |
Product Classification |
Blood and urine collection kit (excludes HIV testing) - Product Code OIB
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Product | Maintenance Flush Kit/Blood Draw
Product Code: DT19335 |
Code Information |
Lot Number Expiration 2018110501 7/31/2021 2018121801 7/31/2021 2019013001 9/30/2021 2019032901 9/30/2021 |
Recalling Firm/ Manufacturer |
Centurion Medical Products Corporation 100 Centurion Way Williamston MI 48895-9086
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For Additional Information Contact | Lisa A. Carpenter 517-545-1156 |
Manufacturer Reason for Recall | Supplier initiated recall of the GRIPPER Needles |
FDA Determined Cause 2 | Nonconforming Material/Component |
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. |
Quantity in Commerce | 240 kits |
Distribution | IL |
Total Product Life Cycle | TPLC Device Report |
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1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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