Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip ARROWg+ard Blue Catheter, Cat. No. AK-22502 Product Usage: The multiple-lumen catheter permits venous access to the central circulation of pediatric patients. The ARROWg+ard antimicrobial surface is intended to help provide protection against catheterrelated infections. The catheter is not intended to be used as a treatment for existing infections, nor is it indicated for long-term use. The use of the 4, 5, and 5.5 Fr. antimicrobial surface catheters in infants weighing less than 2.0, 2.5, and 3.0 kilograms respectively, have not been evaluated. Therefore, the benefits of these catheters in infants weighing less than the indicated weights should be weighed against any possible risks.
FDA Recall Z-2886-2018 · Posted None
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Recalling FirmArrow International Inc
Recall StatusTerminated
Product CodeFOZ
Date Initiated2018-07-03
Date Terminated2020-04-29
Product Quantity166
Reason for Recall
One lot of product is from product code AK-22502 so it contains a 2-lumen, 5 Fr x 5 cm
catheter. However, this product is incorrectly labeled as AK-25502, so the lidstock says it
contains a 2-lumen, 5 Fr x 8 cm catheter. No patient injuries have been reported related to this
issue.
Firm Action
On July 3, 2018, the firm sent out Urgent Medical Device Recall letters to customers. The letter communicated the labeling error.
Affected consignees are instructed to take the following actions:
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.
Root Cause
Employee error
Distribution Pattern
Distributors in MO and UT. Medical facilities in AL, CA, IL, MA, NH, NM, NY, TX, VA, and WI.
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.
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