Date Initiated by Firm | May 09, 2017 |
Create Date | June 12, 2017 |
Recall Status1 |
Terminated 3 on September 17, 2018 |
Recall Number | Z-2336-2017 |
Recall Event ID |
77232 |
510(K)Number | K862056 |
Product Classification |
Catheter, percutaneous - Product Code DQY
|
Product | Arrow Multi-Lumen CVC Kit
The Arrow Two-Lumen Central Venous Access device permits venous access and catheter introduction to the central circulation. |
Code Information |
Material number: CDC-12703-1A, CDC-12802-1A, CDC-15703-1A, CDC-15703-B1A, CDC-15802-1A, Device Listing E426708 |
Recalling Firm/ Manufacturer |
Arrow International Inc 2400 Bernville Rd Reading PA 19605-9607
|
For Additional Information Contact | 610-378-0131 |
Manufacturer Reason for Recall | The Arrow CVC is indicated to provide short-term (<30 days) central venous access for treatment of diseases or conditions requiring central venous access including, but not limited to:
-multiple infusions of fluids, medications, or chemotherapy
-infusion of fluids that are hypertonic, hyperosmolar, or have divergent pH values
-frequent blood sampling or blood/blood components infusions
-infusion of incompatible medications
-central venous pressure monitoring
lack of usable peripheral IV sites
-replacement of multiple peripheral sites for IV access |
FDA Determined Cause 2 | Packaging |
Action | Arrow International sent an Urgent Medical Device Recall Notification Letter dated May 11, 2017, to affected customers. The firm's notification letter is requesting that customers immediately assess their current inventory and to discontinue and quarantine any product with the specific lot codes listed in the letter. In addition, customers were asked to complete the Recall Acknowledgement form and fax or email it back to Customer Service so they can receive a Returns Good Authorization Number for the product's return. Customers with questions were instructed to contact their local sales representative or Customer Service at 1-866-246-6990. |
Quantity in Commerce | 27,485 units distributed in U.S., 4,371 units distributed internationally |
Distribution | Worldwide Distribution - US (nationwide) and Canada |
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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510(K) Database | 510(K)s with Product Code = DQY
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