Date Initiated by Firm |
April 13, 2020 |
Create Date |
May 29, 2020 |
Recall Status1 |
Terminated 3 on November 25, 2020 |
Recall Number |
Z-2176-2020 |
Recall Event ID |
85502 |
Product Classification |
Neurological tray - Product Code OJG
|
Product |
Sterile Custom Packs to be used in surgical procedures. |
Code Information |
ACS Tray Numbers: AGSBOO6K; Lot # 660191, Exp. Date 12/06/2020 (19 kits) AGDB14J; Lot # 737191, Exp. Date 09/20/2020 (2 kits) AHLA17J; Lot # 653191, Exp. Date 12/13/2020 (12 kits) SVNE16K; Lot # 691191, Exp. Date 11/05/2020 (20 kits) WPLA17I; Lot # 685191, Exp. Date 11/11/2020 (2 kits) |
Recalling Firm/ Manufacturer |
American Contract Systems Jackson Pointe Commerce 4050 Jacksons Pointe Ct Zelienople PA 16063-2838
|
For Additional Information Contact |
Steve Theissen 952-926-3515
|
Manufacturer Reason for Recall |
The surgical gowns were manufactured in a facility that is not registered by the FDA.
|
FDA Determined Cause 2 |
Process control |
Action |
Notification to the distributor and instructed them to notify its customers (hospitals) of the recall and product removal. |
Quantity in Commerce |
2868 total kits |
Distribution |
US Nationwide distribution including in the state of Pennsylvania. |
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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