Arrow Three-Lumen CVC Recall: Incorrect Gravity Flow Rates
Arrow recalls specific models of Three-Lumen CVC due to incorrect gravity flow rates on the lidstock. Affected units may not function properly.
Lower-risk recall
Gravity flow rates on the affected product lidstock are incorrect.
Contact the company
What happened, in plain English
Arrow is recalling certain Three-Lumen CVC products because the lidstock has incorrect gravity flow rates. This could lead to improper fluid drainage, potentially causing the device to malfunction. Read more at govinfonow.com/recall/60728-arrow-three-lumen-cvc-recall-incorrect-gravity-flow-rates.
Source Summary by GovInfoNow · govinfonow.com/recall/60728-arrow-three-lumen-cvc-recall-incorrect-gravity-flow-rates · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1290-2022
Cite this page
“Arrow Three-Lumen CVC Recall: Incorrect Gravity Flow Rates.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/60728-arrow-three-lumen-cvc-recall-incorrect-gravity-flow-rates. Based on FDA recall #Z-1290-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1290-2022%22&limit=1).
Why it’s dangerous
The lidstock on the affected products has incorrect gravity flow rates, which can cause improper fluid drainage. This may result in the device not functioning as intended, but it does not pose an immediate risk of injury.
Who’s affected
Users of the recalled Arrow Three-Lumen CVC models with specific lot numbers are affected. Patients using these devices for medical purposes may be at risk of improper fluid drainage.
How to tell if you have this one
Check for the product name 'Arrow Three-Lumen CVC' with catalog number CV-12123-F and specific lot numbers listed in the recall notice.
- Brand
Arrow- Product
Arrow Three-Lumen CVC- Category
Medical device
What to do — step by step
Check Product Details
Identify if your Arrow Three-Lumen CVC has the catalog number CV-12123-F and one of the listed lot numbers.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide distribution in the states 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 2.3 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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-1290-2022 (May 5, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1290-2022 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.