Date Initiated by Firm |
August 16, 2022 |
Date Posted |
September 28, 2022 |
Recall Status1 |
Open3, Classified |
Recall Number |
Z-1824-2022 |
Recall Event ID |
90793 |
Product Classification |
Wire, guide, catheter - Product Code DQX
|
Product |
Amplatz extra Stiff Wire Guide, Stiff Guidewire (OUS ONLY); Reference Part Number: THSF-35-145-AES-SGH (GPN G06801) THSF-38-80-AES-SGH (GPN G06874)
|
Code Information |
THSF-35-145-AES-SGH (GPN G06801) - UDI (01)00827002068018(17)270602(10)14767453 - Lot 14767453, Expiration Date 02-06-2027
THSF-38-80-AES-SGH (GPN G06874) - UDI (01)00827002068742(17)270620(10)14802152
- Lot 14802152, Expiration Date 20-06-2027
|
Recalling Firm/ Manufacturer |
Cook Incorporated 750 N Daniels Way Bloomington IN 47404-9120
|
For Additional Information Contact |
Cook Medical Customer Relations Department 800-457-4500
|
Manufacturer Reason for Recall |
Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.
|
FDA Determined Cause 2 |
Under Investigation by firm |
Action |
On August 16, 2022, Cook Medical notified affected customers of the recall. Customers were instructed to immediately cease all further distribution and use of the affected products. Affected product should be quarantined and returned to Cook Medical to receive product credit.
If you have any questions or concerns, please contact Cook Medical Customer Relations at 800.457.4500 or 812.339.2235 |
Quantity in Commerce |
204 OUS |
Distribution |
Domestic distribution nationwide. Foreign distribution worldwide. |
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 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
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