| Date Initiated by Firm | October 16, 2018 |
| Create Date | November 05, 2019 |
| Recall Status1 |
Terminated 3 on June 15, 2021 |
| Recall Number | Z-0289-2020 |
| Recall Event ID |
83633 |
| 510(K)Number | K810637 |
| Product Classification |
Transducer, blood-pressure, extravascular - Product Code DRS
|
| Product | Argon Medical Devices Double Male LL Adapter, REF 040184800A, bulk, non-sterile. The firm name on the label is Argon Medical Devices, Inc., Athens, TX. |
| Code Information |
Lot number 11229386 |
| FEI Number |
1625425
|
Recalling Firm/ Manufacturer |
Argon Medical Devices, Inc 1445 Flat Creek Rd Athens TX 75751-5002
|
| For Additional Information Contact | Ms. Rebecca Ellis 903-675-9321 |
Manufacturer Reason for Recall | The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product. |
FDA Determined Cause 2 | Equipment maintenance |
| Action | The recalling firm began issuing letters dated 10/16/2018 on 10/16/2018 via registered mail identifying the issue and the action to be taken by the customer. |
| Quantity in Commerce | Total number in recall for all products in dist: 49,130 units |
| Distribution | Distribution was nationwide. There was military/government distribution.
Foreign distribution was made to Canada, Australia, the Netherlands, and Spain. |
| Total Product Life Cycle | TPLC Device Report |
|
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.
|
| 510(K) Database | 510(K)s with Product Code = DRS
|