Lower riskMedical device recall · FDA · Published September 14, 2022
ARROW Pressure Injectable Arrowg+ard Blue Advance Kit Mislabeled - Risk of Incorrect Use
ARROW recalls a specific midline IV kit due to mislabeled catheter size. This could lead to incorrect use if the wrong catheter is used. Affected units have a specific product code and reference number.
Mislabeling: the corrugate label, lidstock, banner card, and peel sticker accompanying the affected product incorrectly displays a double lumen 5.5 French catheter (and related priming volumes and kit contents for product code ASK-41552-JHVA1), instead of the packaged single-lumen 4.5 French catheter (and related priming volumes and kit contents for product code ASK-41541-JHVA1).
“ARROW Pressure Injectable Arrowg+ard Blue Advance Kit Mislabeled - Risk of Incorrect Use.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/60059-arrow-pressure-injectable-arrowg-ard-blue-advance-kit-mislabeled-risk. Based on FDA recall #Z-0102-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0102-2023%22&limit=1).
The FDA announced on Sept. 14, 2022, that ARROW INTERNATIONAL Inc. recalled its ARROW Pressure Injectable Arrowg+ard Blue Advance Two-Lumen Midline Kit due to mislabeling that incorrectly displays a double lumen catheter instead of the packaged single-lumen device. The recall affects 18 units distributed in Florida.
How to tell if you have it
ARROW Pressure Injectable Arrowg+ard Blue Advance Two-Lumen Midline Kit, 5.5 Fr, 15 cm, .018 Inch dia., REF ASK-41552-JHVA1
UPC: 10801902144284
The hazard
The corrugate label, lidstock, banner card, and peel sticker accompanying the affected product incorrectly display a double lumen 5.5 French catheter and related kit contents for product code ASK-41552-JHVA1, instead of the packaged single-lumen 4.5 French catheter and related contents for product code ASK-41541-JHVA1.
Context
GovInfoNow's records show ARROW INTERNATIONAL Inc. has 52 other recalls on record since June 1, 2017. Recent recalls include Arrow Arterial Kits and Trays (July 26, 2024) regarding open seals, the Arrow Ultra 8 IAB Catheter Kit (April 29, 2024) for potential serious health consequences, and the ARROW QuickFlash Radial Artery Catheter (Feb. 12, 2024) due to a potentially defective component. Other recent recalls of similar products include Arrow Pressure Injectable Arrowg+ard Blue Plus Four-Lumen CVC Kit, Arrowg+ard Blue MAC Two-Lumen Catheter Kit, and Arrow Pressure Injectable Catheters, all dated March 11, 2026, for incorrect adhesive manufacturing.
How to tell if you have this one
Check for the product code ASK-41552-JHVA1 on the label or packaging. The kit includes a specific catheter size (5.5 Fr, 15 cm) and is part of the Arrowg+ard Blue Advance series.
Brand
ARROW
Product
ARROW Pressure Injectable Arrowg+ard Blue Advance Two-Lumen Midline Kit, 5.5 Fr, 15 cm, .018 Inch dia., REF
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the product code ASK-41552-JHVA1 on the label or packaging to confirm if the kit is affected.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution in the state of Florida.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 16 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0102-2023 (September 14, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0102-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.