Arrow AGB + Multi-Lumen CVC Kit, Cat. No. CDC-42703-B1A. Product Usage - The Arrow CVC is intended to provide short-term (< 30 days) central venous access for treatment of diseases or conditions requiring central venous access, including, but not limited to the following: Lack of usable peripheral IV sites, Central venous pressure monitoring, Total parenteral nutrition (TPN), Infusions of fluids, medications, or chemotherapy, and Frequent blood sampling or receiving blood transfusions/blood products.
FDA Recall Z-0282-2019 · Posted None
Advertisement
Recalling FirmArrow International Inc
Recall StatusTerminated
Product CodeFOZ
Date Initiated2018-08-30
Date Terminated2020-07-31
Product Quantity105
Reason for Recall
The product was
shipped after its expiry date due to a system error. The product lidstock identifies the
correct expiration date however the accompanying purchase order shipping
documentation identifies an incorrect expiration date. Per standard clinical practice the
lidstock would most likely be checked prior to use and the product would not be used
leading to a minor delay while a replacement is located. In the unlikely event that the
product lidstock is not checked prior to use, there is potential for use of expired
product, and product functionality/or sterility cannot be guaranteed.
Firm Action
On August 29, 2018, the firm notified customers via an Urgent Medical Device Recall letter. The letter informed customers of the product issue.
Customers were advised to do the following:
1. If you have affected stock, immediately discontinue use and quarantine any products with the product code and lot number listed above, so that the affected products can be returned to Arrow.
2. To return product, complete the enclosed Recall Acknowledgement Form and fax it to 1-855-419-8507, Attn: Customer Service or email to [email protected]. This will allow us to document the amount of product you have on hand for return. A customer service representative will contact you with a Return Goods Authorization (RGA) Number and will provide instructions for the return of products to Arrow International.
3. If you have no affected stock, please complete the enclosed Recall Acknowledgment Form and fax it to 1-855-419-8507, Attn: Customer Service or email to [email protected]. This will allow us to document your receipt of this letter.
If you have any other questions, feel free to contact your local sales representative or Customer Service at 1-866-396-2111.
Root Cause
Under Investigation by firm
Distribution Pattern
US nationwide in the states of CA, FL, NC, and RI.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
Advertisement